Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

出版年份 2015 全文链接

标题

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

作者

关键词

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出版物

AMERICAN JOURNAL OF HUMAN GENETICS

Volume 97, Issue 2, Pages 343-352

出版商

Elsevier BV

发表日期

2015-07-31

DOI

10.1016/j.ajhg.2015.07.004

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