Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.
Bilgüvar K; Oztürk AK; Louvi A; Kwan KY; Choi M; Tatli B; Yalnizoğlu D; Tüysüz B; Cağlayan AO; Gökben S; Kaymakçalan H; Barak T; Bakircioğlu M; Yasuno K; Ho W; Sanders S; Zhu Y; Yilmaz S; Dinçer A; Johnson MH; Bronen RA; Koçer N; Per H; Mane S; Pamir MN; Yalçinkaya C; Kumandaş S; Topçu M; Ozmen M; Sestan N; Lifton RP; State MW; Günel M; Nature, 2010, vol. 467, issue 7312, p 207, ISSN 14764687. ISBN 14764687.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef