Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
Kaya Bilgüvar(Yale University), Ali K. Ozturk(Yale University), Angeliki Louvi(Center for Human Genetics), Kenneth Y. Kwan(Yale University), Murim Choi(Center for Human Genetics), Burak Tatli(Istanbul University), Dilek Yalnızoğlu(Hacettepe University), Beyhan Tüysüz(Istanbul University-Cerrahpaşa), Ahmet Okay Çağlayan(Kayseri Eğitim ve Araştırma Hastanesi), Sarenur Gökben(Ege University), Hande Kaymakçalan(Bahçeşehir University), Tanyeri Barak(Yale University), Mehmet Bakırcıoğlu(Yale University), Katsuhito Yasuno(Yale University), Winson S. Ho(Center for Human Genetics), Stephan Sanders(Center for Human Genetics), Ying Zhu(Yale University), Sanem Yılmaz(Ege University), Alp Di̇nçer(Acıbadem University), Michele H. Johnson(Yale University), Richard A. Bronen(Yale University), Naci Koçer(Istanbul University-Cerrahpaşa), Hüseyin Per(Erciyes University), Shrikant Mane(Center for Human Genetics), M. Necmettin Pamir(Acıbadem University), Cengiz Yalçınkaya(Istanbul University), Sefer Kumandaş(Erciyes University), Meral Topçu(Hacettepe University), Meral Özmen(Istanbul University), Nenad Šestan(Yale University), Richard P. Lifton(Yale University), Matthew W. State(Center for Human Genetics), Murat Günel(Center for Human Genetics)
Cited by 496Open Access