Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.
Bilgüvar, Kaya; Öztürk, Ali Kemal; Louvi, Angeliki; Kwan, Kenneth Y.; Choi, Murim; Tatlı, Burak; Yalnızoğlu, Dilek; Tüysüz, Beyhan; Çağlayan, Ahmet Okay; Gökben, Sarenur; Kaymakçalan, Hande; Barak, Tanyeri; Bakırcıoğlu, Mehmet; Yasuno, Katsuhito; Winson Ho; Sanders, Stephan; Ying Zhu; Yılmaz, Sanem; Dinçer, Alp; Johnson, Michele H.; Nature, 2010, vol. 467, issue 7312, p 207, ISSN 00280836. ISBN 00280836.

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