Vitamin D as an adjunct to subcutaneous allergen immunotherapy in asthmatic children sensitized to house dust mite by Baris, S., Kiykim, A., Ozen, A., Tulunay, A., Karakoc‐Aydiner, E., Barlan, I. B.

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JAGN1 Deficient Severe Congenital Neutropenia: Two Cases from the Same Family by Baris, S., Karakoc–Aydiner, E., Ozen, A., Delil, K., Kiykim, A., Ogulur, I., Baris, I., Barlan, I. B.

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Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score by Tesch, Victoria Katharina, Abolhassani, Hassan, Shadur, Bella, Zobel, Joachim, Mareika, Yuliya, Sharapova, Svetlana, Karakoc-Aydiner, Elif, Rivière, Jacques G., Garcia-Prat, Marina, Moes, Nicolette, Haerynck, Filomeen, Gonzales-Granado, Luis I., Santos Pérez, Juan Luis, Mukhina, Anna, Shcherbina, Anna, Aghamohammadi, Asghar, Hammarström, Lennart, Dogu, Figen, Haskologlu, Sule, İkincioğulları, Aydan İ., Köstel Bal, Sevgi, Baris, Safa, Kilic, Sara Sebnem, Karaca, Neslihan Edeer, Kutukculer, Necil, Girschick, Hermann, Kolios, Antonios, Keles, Sevgi, Uygun, Vedat, Stepensky, Polina, Worth, Austen, van Montfrans, Joris M., Peters, Anke M.J., Meyts, Isabelle, Adeli, Mehdi, Marzollo, Antonio, Padem, Nurcicek, Khojah, Amer M., Chavoshzadeh, Zahra, Avbelj Stefanija, Magdalena, Bakhtiar, Shahrzad, Florkin, Benoit, Meeths, Marie, Gamez, Laura, Grimbacher, Bodo, Seppänen, Mikko R.J., Lankester, Arjan, Gennery, Andrew R., Seidel, Markus G.

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Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syn... by Maccari, Maria Elena, Abolhassani, Hassan, Aghamohammadi, Asghar, Aiuti, Alessandro, Aleinikova, Olga, Bangs, Catherine, Baris, Safa, Barzaghi, Federica, Baxendale, Helen, Buckland, Matthew, Burns, Siobhan O, Cancrini, Caterina, Cant, Andrew, Cathébras, Pascal, Cavazzana, Marina, Chandra, Anita, Conti, Francesca, Coulter, Tanya, Devlin, Lisa A, Edgar, J David M, Faust, Saul, Fischer, Alain, Garcia-Prat, Marina, Hammarström, Lennart, Heeg, Maximilian, Jolles, Stephen, Karakoc-Aydiner, Elif, Kindle, Gerhard, Kiykim, Ayca, Kumararatne, Dinakantha, Grimbacher, Bodo, Longhurst, Hilary, Mahlaoui, Nizar, Milota, Tomas, Moreira, Fernando, Moshous, Despina, Mukhina, Anna, Neth, Olaf, Neven, Benedicte, Nieters, Alexandra, Olbrich, Peter, Ozen, Ahmet, Pachlopnik Schmid, Jana, Picard, Capucine, Prader, Seraina, Rae, William, Reichenbach, Janine, Rusch, Stephan, Savic, Sinisa, Scarselli, Alessia, Scheible, Raphael, Sediva, Anna, Sharapova, Svetlana O, Shcherbina, Anna, Slatter, Mary, Soler-Palacin, Pere, Stanislas, Aurelie, Suarez, Felipe, Tucci, Francesca, Uhlmann, Annette, van Montfrans, Joris, Warnatz, Klaus, Williams, Anthony Peter, Wood, Phil, Kracker, Sven, Condliffe, Alison Mary, Ehl, Stephan

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Expanding the Clinical and Immunological Phenotypes and Natural History of MALT1 Deficiency by Sefer, Asena Pinar, Abolhassani, Hassan, Ober, Franziska, Kayaoglu, Basak, Bilgic Eltan, Sevgi, Kara, Altan, Erman, Baran, Surucu Yilmaz, Naz, Aydogmus, Cigdem, Aydemir, Sezin, Charbonnier, Louis-Marie, Kolukisa, Burcu, Azizi, Gholamreza, Delavari, Samaneh, Momen, Tooba, Aliyeva, Simuzar, Kendir Demirkol, Yasemin, Tekin, Saban, Kiykim, Ayca, Baser, Omer Faruk, Cokugras, Haluk, Gursel, Mayda, Karakoc-Aydiner, Elif, Ozen, Ahmet, Krappmann, Daniel, Chatila, Talal A., Rezaei, Nima, Baris, Safa

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DOCK8 Deletions and Mutations Are Associated With The Autosomal Recessive Hyper-IgE Phenotype by McGhee, S.A, Engelhardt, K, Winkler, S, Sassi, A, Woellner, C, Lopez-Herrera, G, Chen, A, Kim, H, Lloret, M. Garcia, Schulze, I, Ehl, S, Thiel, J, Pfeifer, D, Veelken, H, Niehues, T, Siepermann, K, Weinspach, S, Reisli, I, Keles, S, Genel, F, Kütükçüler, N, Camcioglu, Y, Somer, A, Karakoc-Aydiner, E, Barlan, I

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Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency by Ghosh, Sujal, Köstel Bal, Sevgi, Edwards, Emily S.J., Pillay, Bethany, Jiménez Heredia, Raúl, Erol Cipe, Funda, Rao, Geetha, Salzer, Elisabeth, Zoghi, Samaneh, Abolhassani, Hassan, Momen, Tooba, Gostick, Emma, Price, David A., Zhang, Yu, Oler, Andrew J., Gonzaga-Jauregui, Claudia, Erman, Baran, Metin, Ayse, Ilhan, Inci, Haskologlu, Sule, Islamoglu, Candan, Baskin, Kubra, Ceylaner, Serdar, Yilmaz, Ebru, Unal, Ekrem, Karakukcu, Musa, Berghuis, Dagmar, Cole, Theresa, Gupta, Aditya K., Hauck, Fabian, Kogler, Hubert, Hoepelman, Andy I.M., Baris, Safa, Karakoc-Aydiner, Elif, Ozen, Ahmet, Kager, Leo, Holzinger, Dirk, Paulussen, Michael, Krüger, Renate, Meisel, Roland, Oommen, Prasad T., Morris, Emma, Neven, Benedicte, Worth, Austen, van Montfrans, Joris, Fraaij, Pieter L.A., Choo, Sharon, Dogu, Figen, Davies, E. Graham, Burns, Siobhan, Dückers, Gregor, Becker, Ruy Perez, von Bernuth, Horst, Latour, Sylvain, Faraci, Maura, Gattorno, Marco, Su, Helen C., Pan-Hammarström, Qiang, Hammarström, Lennart, Lenardo, Michael J., Ma, Cindy S., Niehues, Tim, Aghamohammadi, Asghar, Rezaei, Nima, Ikinciogullari, Aydan, Tangye, Stuart G., Lankester, Arjan C., Boztug, Kaan

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Consensus Middle East and North Africa Registry on Inborn Errors of Immunity by Aghamohammadi, Asghar, Rezaei, Nima, Yazdani, Reza, Delavari, Samaneh, Kutukculer, Necil, Topyildiz, Ezgi, Ozen, Ahmet, Baris, Safa, Karakoc-Aydiner, Elif, Kilic, Sara Sebnem, Kose, Hulya, Gulez, Nesrin, Genel, Ferah, Reisli, Ismail, Djenouhat, Kamel, Tahiat, Azzeddine, Boukari, Rachida, Ladj, Samir, Belbouab, Reda, Ferhani, Yacine, Belaid, Brahim, Djidjik, Reda, Kechout, Nadia, Attal, Nabila, Saidani, Khalissa, Barbouche, Ridha, Bousfiha, Aziz, Sobh, Ali, Rizk, Ragheed, Elnagdy, Marwa H., Al-Ahmed, Mona, Al-Tamemi, Salem, Nasrullayeva, Gulnara, Adeli, Mehdi, Al-Nesf, Maryam, Hassen, Amel, Mehawej, Cybel, Irani, Carla, Megarbane, Andre, Quinn, Jessica, Maródi, László, Modell, Vicki, Modell, Fred, Al-Herz, Waleed, Geha, Raif S., Abolhassani, Hassan

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Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity by Wolkewitz, Martin, Schwab, Charlotte, Lorenzini, Tiziana, Leiding, Jennifer W., Aladjdi, Nathalie, Abou-Chahla, Wadih, Baris, Safa, Barlogis, Vincent, Barzaghi, Federica, Baumann, Ulrich, Bloomfield, Marketa, Bohynikova, Nadezda, Bodet, Damien, Burns, Siobhan O., Cathébras, Pascal, Ekwall, Olov, Frange, Pierre, Geier, Christoph, Goda, Vera, Hammarström, Lennart, Hauck, Fabian, Heropolitanska-Pliszka, Edyta, Jolles, Stephen, Karakoc-Aydiner, Elif, Kindle, Gerhard R., Klemann, Christian, Koltan, Sylwia, Krüger, Renate, Jeziorski, Eric, Lougaris, Vassilios, Marzollo, Antonio, Mahlaoui, Nizar, Malphettes, Marion, Meinhardt, Andrea, Merlin, Etienne, Meyts, Isabelle, Milota, Tomas, Moshous, Despina, Mukhina, Anna, Neven, Benedicte, Nieters, Alexandra, Nove-Josserand, Raphaele, Oksenhendler, Eric, Ozen, Ahmet, Olbrich, Peter, Pac, Malgorzata, Parra-Martinez, Alba, Paschenko, Olga, Prader, Seraina, Raffray, Loic, Ritterbusch, Henrike, Riviere, Jacques G., Rusch, Stephan, Sakovich, Inga, Savic, Sinisa, Schuetz, Catharina, Schulz, Ansgar, Sediva, Anna, Semeraro, Michaela, Slatter, Mary A., Stephan, Jean-Louis, Suarez, Felipe, Trück, Johannes, van Aerde, Koen J., von Bernuth, Horst, Warnatz, Klaus, Ip, Winnie, Picard, Capucine, Grimbacher, Bodo, Kracker, Sven, Condliffe, Alison M., Ehl, Stephan, Gennery, Andrew, Tantou, Sofia, Grigoriadou, Sofia, Cericola, Gabriella, Scheibenbogen, Carmen, Krivan, Gergely, McGuire, Frances K., Leahy, Timothy Ronan, Edgar, John David M., Bakhtiar, Shahrzad, Bader, Peter, Rohner, Geraldine Blanchard, Haerynck, Filomeen, Claes, Karlien, Fasshauer, Maria, Graf, Dagmar, Jeseňák, Miloš, Fabio, Giovanna, Giardino, Giuliana, Karadağ, Ilknur Kökçü, Yıldıran, Alişan, Steinmann, Sandra, Pietrucha, Barbara Maria, Gernert, Michael, Witte, Torsten, Wolska-Kusnierz, Beata, Zabara, Dariia V., Shvets, Oksana A.

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Clinical, immunological, molecular and therapeutic findings in monogenic immune dysregulation diseases: Middle East and North Africa registry by Jamee, Mahnaz, Azizi, Gholamreza, Baris, Safa, Karakoc-Aydiner, Elif, Ozen, Ahmet, Kiliç, Sara Ş., Kose, Hulya, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Momen, Tooba, Shamsian, Bibi Shahin, Fallahi, Mazdak, Sharafian, Samin, Gülez, Nesrin, Aygun, Ayşe, Karaca, Neslihan Edeer, Kutukculer, Necil, Al Sukait, Nashat, Al Farsi, Tariq, Al-Tamemi, Salem, Khalifa, Nisreen, Shereen, Reda, El-Ghoneimy, Dalia, El-Owaidy, Rasha, Radwan, Nesrine, Alzyoud, Raed, Barbouche, Mohamed-Ridha, Ben-Mustapha, Imen, Mekki, Najla, Rais, Afef, Boukari, Rachida, Belbouab, Reda, Djenouhat, Kamel, Tahiat, Azzeddine, Touri, Souad, Elghazali, Gehad, Al-Hammadi, Suleiman, Shendi, Hiba Mohammed, Alkuwaiti, Amna, Belaid, Brahim, Djidjik, Reda, Artac, Hasibe, Adeli, Mehdi, Sobh, Ali, Elnagdy, Marwa H., Bahgat, Sara A., Nasrullayeva, Gulnara, Chou, Janet, Rezaei, Nima, Al-Herz, Waleed, Geha, Raif S., Abolhassani, Hassan, Rasouli, Seyed Erfan, Esmaeili, Marzie, Yazdani, Reza, Delavari, Samaneh, Tavakol, Marzieh, Sadri, Homa, Karimi, Abdollah, Shiari, Reza, Alavi, Samin, Babaie, Delara, Eshghi, Peyman, Armin, Shahnaz, Vosughimotlagh, Ahmad, Eltan, Sevgi Bilgic, Babayeva, Royala, Sefer, Asena Pinar, Kolukisa, Burcu, Gungoren, Ezgi Yalcin, Altunbas, Melek Yorgun, Mammadova, Vafa

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Clinical and immunological outcomes of SARS-CoV-2 infection in patients with inborn errors of immunity receiving different brands and doses of COVID-19 vaccines by Karabiber, Esra, Atik, Özge, Tepetam, Fatma Merve, Ergan, Bilgehan, İlki, Arzu, Karakoç Aydıner, Elif, Özen, Ahmet, Özyer, Fatma, Barış, Safa

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Treatment forms and clinical course of LPS-Responsive beige-like anchor protein deficiency and introduction of the immune deficiency and -dysregulation activity (=IDDA) score by Tesch, VK, Abolhassani, H, Grimbacher, B, Lankaster, A, Gennery, A, Shadur, B, Stepensky, P, Mareika, Y, Sharapova, S, Karakoc-Aydiner, E, Riviere, JG, Garcia-Prat, M, Moes, N, Haerynck, F, Gonzales-Granado, LI, Perez, JLS, Mukhina, A, Aghamohammadi, A, Hammarstrom, L, Dogu, F, Ikinciogullari, AI, Bal, S, Baris, S, Kilic, SS, Karaca, NE, Kutukculer, N, Girschick, H, Kolios, A, Keles, S, Seidel, MG

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TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome by Werren, Elizabeth A., LaForce, Geneva R., Srivastava, Anshika, Perillo, Delia R., Li, Shaokun, Johnson, Katherine, Baris, Safa, Berger, Brandon, Regan, Samantha L., Pfennig, Christian D., de Munnik, Sonja, Pfundt, Rolph, Hebbar, Malavika, Jimenez-Heredia, Raúl, Karakoc-Aydiner, Elif, Ozen, Ahmet, Dmytrus, Jasmin, Krolo, Ana, Corning, Ken, Prijoles, E. J., Louie, Raymond J., Lebel, Robert Roger, Le, Thuy-Linh, Amiel, Jeanne, Gordon, Christopher T., Boztug, Kaan, Girisha, Katta M., Shukla, Anju, Bielas, Stephanie L., Schaffer, Ashleigh E.

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Coronavirus disease 2019 in patients with inborn errors of immunity: An international study by Meyts, Isabelle, Bucciol, Giorgia, Quinti, Isabella, Neven, Bénédicte, Fischer, Alain, Seoane, Elena, Lopez-Granados, Eduardo, Gianelli, Carla, Robles-Marhuenda, Angel, Jeandel, Pierre-Yves, Paillard, Catherine, Sankaran, Vijay G., Demirdag, Yesim Yilmaz, Lougaris, Vassilios, Aiuti, Alessandro, Plebani, Alessandro, Milito, Cinzia, Dalm, Virgil ASH, Guevara-Hoyer, Kissy, Sánchez-Ramón, Silvia, Bezrodnik, Liliana, Barzaghi, Federica, Gonzalez-Granado, Luis Ignacio, Hayman, Grant R., Uzel, Gulbu, Mendonça, Leonardo Oliveira, Agostini, Carlo, Spadaro, Giuseppe, Badolato, Raffaele, Soresina, Annarosa, Vermeulen, François, Bosteels, Cedric, Lambrecht, Bart N., Keller, Michael, Mustillo, Peter J., Abraham, Roshini S., Gupta, Sudhir, Ozen, Ahmet, Karakoc-Aydiner, Elif, Baris, Safa, Freeman, Alexandra F., Yamazaki-Nakashimada, Marco, Scheffler-Mendoza, Selma, Espinosa-Padilla, Sara, Gennery, Andrew R., Jolles, Stephen, Espinosa, Yazmin, Poli, M. Cecilia, Fieschi, Claire, Hauck, Fabian, Cunningham-Rundles, Charlotte, Mahlaoui, Nizar, Warnatz, Klaus, Sullivan, Kathleen E., Tangye, Stuart G.

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Therapeutic options for CTLA-4 insufficiency by Egg, David, Rump, Ina Caroline, Mitsuiki, Noriko, Rojas-Restrepo, Jessica, Maccari, Maria-Elena, Schwab, Charlotte, Gabrysch, Annemarie, Warnatz, Klaus, Goldacker, Sigune, Patiño, Virginia, Wolff, Daniel, Okada, Satoshi, Hayakawa, Seiichi, Shikama, Yoshiaki, Kanda, Kenji, Imai, Kohsuke, Sotomatsu, Manabu, Kuwashima, Makoto, Kamiya, Takahiro, Morio, Tomohiro, Matsumoto, Kazuaki, Mori, Takeshi, Yoshimoto, Yuri, Dybedal, Ingunn, Kanariou, Maria, Kucuk, Zeynep Yesim, Chapdelaine, Hugo, Petruzelkova, Lenka, Lorenz, Hanns-Martin, Sullivan, Kathleen E., Heimall, Jennifer, Moutschen, Michel, Litzman, Jiri, Recher, Mike, Albert, Michael H., Hauck, Fabian, Seneviratne, Suranjith, Pachlopnik Schmid, Jana, Kolios, Antonios, Unglik, Gary, Klemann, Christian, Snapper, Scott, Giulino-Roth, Lisa, Svaton, Michael, Platt, Craig D., Hambleton, Sophie, Neth, Olaf, Gosse, Geraldine, Reinsch, Steffen, Holzinger, Dirk, Kim, Yae-Jean, Bakhtiar, Shahrzad, Atschekzei, Faranaz, Schmidt, Reinhold, Sogkas, Georgios, Chandrakasan, Shanmuganathan, Rae, William, Derfalvi, Beata, Marquart, Hanne Vibeke, Ozen, Ahmet, Kiykim, Ayca, Karakoc-Aydiner, Elif, Králíčková, Pavlína, de Bree, Godelieve, Kiritsi, Dimitra, Seidel, Markus G., Kobbe, Robin, Dantzer, Jennifer, Alsina, Laia, Armangue, Thais, Lougaris, Vassilios, Agyeman, Philipp, Nyström, Sofia, Buchbinder, David, Arkwright, Peter D., Grimbacher, Bodo

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Disease evolution and response to rapamycin in Activated Phosphoinositide 3-Kinase δ syndrome: the european society for immunodeficiencies-Activated Phosphoinositide 3-Kinase d syn... by Maccari, ME, Abolhassani, H, Aghamohammadi, A, Aiuti, A, Aleinikova, O, Bangs, C, Baris, S, Barzaghi, F, Baxendale, H, Buckland, M

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Evaluating the efficacy and safety of pozelimab in patients with CD55 deficiency with hyperactivation of complement, angiopathic thrombosis, and protein-losing enteropathy disease:... by Ozen, Ahmet, Chongsrisawat, Voranush, Sefer, Asena Pinar, Kolukisa, Burcu, Jalbert, Jessica J, Meagher, Karoline A, Brackin, Taylor, Feldman, Hagit Baris, Baris, Safa, Karakoc-Aydiner, Elif, Ergelen, Rabia, Fuss, Ivan J, Moorman, Heather, Suratannon, Narissara, Suphapeetiporn, Kanya, Perlee, Lorah, Harari, Olivier A, Yancopoulos, George D, Lenardo, Michael J, Miller, Jutta L., Eshach Adiv, Orly, Bilgic Eltan, Sevgi, Yorgun Altunbas, Melek, Magliocco, Mary, Matthews, Helen, Marciano, Beatriz E., Chatchatee, Pantipa, Trbovic, Caryn F., Burczynski, Michael E., Chaudhari, Umesh, Usta, Yusuf, Altuntaş, Cansu, Yavuz, Sibel, Baştürk, Ahmet, Demirbaş Ar, Fatma, Topal, Erdem, Kalaycı, Ayhan Gazi, Weerapakorn, Wanlapa, Calabi Martínez, Ana Andrea, Bottero, Adriana

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The Notch1/CD22 signaling axis disrupts Treg function in SARS-CoV-2-associated multisystem inflammatory syndrome in children by Benamar, Mehdi, Chen, Qian, Chou, Janet, Julé, Amélie M, Boudra, Rafik, Contini, Paola, Crestani, Elena, Lai, Peggy S, Wang, Muyun, Fong, Jason, Rockwitz, Shira, Lee, Pui, Chan, Tsz Man Fion, Altun, Ekin Zeynep, Kepenekli, Eda, Karakoc-Aydiner, Elif, Ozen, Ahmet, Boran, Perran, Aygun, Fatih, Onal, Pinar, Sakalli, Ayse Ayzit Kilinc, Cokugras, Haluk, Gelmez, Metin Yusuf, Oktelik, Fatma Betul, Cetin, Esin Aktas, Zhong, Yuelin, Taylor, Maria Lucia, Irby, Katherine, Halasa, Natasha B, Mack, Elizabeth H, Signa, Sara, Prigione, Ignazia, Gattorno, Marco, Cotugno, Nicola, Amodio, Donato, Geha, Raif S, Son, Mary Beth, Newburger, Jane, Agrawal, Pankaj B, Volpi, Stefano, Palma, Paolo, Kiykim, Ayca, Randolph, Adrienne G, Deniz, Gunnur, Baris, Safa, De Palma, Raffaele, Schmitz-Abe, Klaus, Charbonnier, Louis-Marie, Henderson, Lauren A, Chatila, Talal A

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Outcomes of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome by Labrosse, Roxane, Chu, Julia I., Armant, Myriam A., Everett, John K., Pellin, Danilo, Kareddy, Niharika, Frelinger, Andrew L., Henderson, Lauren A., O’Connell, Amy E., Biswas, Amlan, Coenen-van der Spek, Jet, Miggelbrink, Alexandra, Fiorini, Claudia, Adhikari, Hriju, Berry, Charles C., Cantu, Vito Adrian, Fong, Johnson, Jaroslavsky, Jason, Karadeniz, Derin F., Li, Quan-Zhen, Reddy, Shantan, Roche, Aoife M., Zhu, Chengsong, Whangbo, Jennifer S., Dansereau, Colleen, Mackinnon, Brenda, Morris, Emily, Koo, Stephanie M., London, Wendy B., Baris, Safa, Ozen, Ahmet, Karakoc-Aydiner, Elif, Despotovic, Jenny M., Forbes Satter, Lisa R., Saitoh, Akihiko, Aizawa, Yuta, King, Alejandra, Nguyen, Mai Anh Thi, Vu, Vy Do Uyen, Snapper, Scott B., Galy, Anne, Notarangelo, Luigi D., Bushman, Frederic D., Williams, David A., Pai, Sung-Yun

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Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis by Kostel Bal, Sevgi, Giuliani, Sarah, Block, Jana, Repiscak, Peter, Hafemeister, Christoph, Shahin, Tala, Kasap, Nurhan, Ransmayr, Bernhard, Miao, Yirun, van de Wetering, Cheryl, Frohne, Alexandra, Jimenez Heredia, Raul, Schuster, Michael, Zoghi, Samaneh, Hertlein, Vanessa, Thian, Marini, Bykov, Aleksandr, Babayeva, Royala, Bilgic Eltan, Sevgi, Karakoc-Aydiner, Elif, Shaw, Lisa E, Chowdhury, Iftekhar, Varjosalo, Markku, Argüello, Rafael J, Farlik, Matthias, Ozen, Ahmet, Serfling, Edgar, Dupré, Loïc, Bock, Christoph, Halbritter, Florian, Hannich, J Thomas, Castanon, Irinka, Kraakman, Michael J, Baris, Safa, Boztug, Kaan

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