A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility by Meindl, Katrin, Issler, Naomi, Afonso, Sara, Cebrian-Serrano, Alberto, Müller, Karin, Sterner, Christina, Othmen, Helga, Tegtmeier, Ines, Witzgall, Ralph, Klootwijk, Enriko, Davies, Benjamin, Kleta, Robert, Warth, Richard

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CLN7/MFSD8 may be an important factor for SARS-CoV-2 cell entry by Heinl, Elena-Sofia, Lorenz, Sebastian, Schmidt, Barbara, Nasser M Laqtom, Nouf, Mazzulli, Joseph R., Francelle, Laetitia, Yu, Timothy W., Greenberg, Benjamin, Storch, Stephan, Tegtmeier, Ines, Othmen, Helga, Maurer, Katja, Steinfurth, Malin, Witzgall, Ralph, Milenkovic, Vladimir, Wetzel, Christian H., Reichold, Markus

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A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness by Issler, Naomi, Afonso, Sara, Weissman, Irith, Jordan, Katrin, Cebrian-Serrano, Alberto, Meindl, Katrin, Dahlke, Eileen, Tziridis, Konstantin, Yan, Guanhua, Robles-López, José M, Tabernero, Lydia, Patel, Vaksha, Kesselheim, Anne, Klootwijk, Enriko D, Stanescu, Horia C, Dumitriu, Simona, Iancu, Daniela, Tekman, Mehmet, Mozere, Monika, Jaureguiberry, Graciana, Outtandy, Priya, Russell, Claire, Forst, Anna-Lena, Sterner, Christina, Heinl, Elena-Sofia, Othmen, Helga, Tegtmeier, Ines, Reichold, Markus, Schiessl, Ina Maria, Limm, Katharina, Oefner, Peter, Witzgall, Ralph, Fu, Lifei, Theilig, Franziska, Schilling, Achim, Shuster Biton, Efrat, Kalfon, Limor, Fedida, Ayalla, Arnon-Sheleg, Elite, Ben Izhak, Ofer, Magen, Daniella, Anikster, Yair, Schulze, Holger, Ziegler, Christine, Lowe, Martin, Davies, Benjamin, Böckenhauer, Detlef, Kleta, Robert, Falik Zaccai, Tzipora C, Warth, Richard

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