De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability

标题
De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 94, Issue 4, Pages 618-624
出版商
Elsevier BV
发表日期
2014-03-28
DOI
10.1016/j.ajhg.2014.03.006

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