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Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies
by
Hammarsjö, A.
,
Wang, Z.
,
Vaz, R.
,
Taylan, F.
,
Sedghi, M.
,
Girisha, K. M.
,
Chitayat, D.
,
Neethukrishna, K.
,
Shannon, P.
,
Godoy, R.
,
Gowrishankar, K.
,
Lindstrand, A.
,
Nasiri, J.
,
Baktashian, M.
,
Newton, P. T.
,
Guo, L.
,
Hofmeister, W.
,
Pettersson, M.
,
Chagin, A. S.
,
Nishimura, G.
,
Yan, L.
,
Matsumoto, N.
,
Nordgren, A.
,
Miyake, N.
,
Grigelioniene, G.
,
Ikegawa, S.
Published in
Scientific reports
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Association of Paraoxonase-1 Genotype and Phenotype with Angiogram Positive Coronary Artery Disease
by
Soflaei, Sara Saffar
,
Baktashian, Mojtaba
,
Moghaddam, Kiana Hosseinpour
,
Saberi-Karimian, Maryam
,
Kosari, Negin
,
Hashemi, Seyed Mohammad
,
Mouhebati, Mohsen
,
Amini, Mahsa
,
Dehghani, Mashallah
,
Esmaily, Habibollah
,
Ebrahimi, Mahmoud
,
Falsoleiman, Homa
,
Nosrati-Tirkani, Abolfazl
,
Sadabadi, Fatemeh
,
Ferns, Gordon A
,
Salehi, Mansoor
,
Pasdar, Alireza
,
Ghayour-Mobarhan, Majid
Published in
Arquivos brasileiros de cardiologia
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Recessive Charcot-Marie-Tooth and multiple sclerosis associated with a variant in MCM3AP
by
Sedghi, Maryam
,
Moslemi, Ali-Reza
,
Cabrera-Serrano, Macarena
,
Ansari, Behnaz
,
Ghasemi, Majid
,
Baktashian, Mojtaba
,
Fattahpour, Ali
,
Tajsharghi, Homa
Published in
Brain communications
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