Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations by Lifton, Richard P, State, Matthew W, Günel, Murat, Bilgüvar, Kaya, Öztürk, Ali Kemal, Louvi, Angeliki, Kwan, Kenneth Y, Choi, Murim, Tatl, Burak, Yaln zo lu, Dilek, Tüysüz, Beyhan, Ça layan, Ahmet Okay, Gökben, Sarenur, Kaymakçalan, Hande, Barak, Tanyeri, Bak rc o lu, Mehmet, Yasuno, Katsuhito, Ho, Winson, Sanders, Stephan, Zhu, Ying, Y lmaz, Sanem, Dinçer, Alp, Johnson, Michele H, Bronen, Richard A, Koçer, Naci, Per, Hüseyin, Mane, Shrikant, Pamir, Mehmet Necmettin, Yalç nkaya, Cengiz, Kumanda, Sefer, Topçu, Meral, Özmen, Meral, Šestan, Nenad

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