Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability

标题
Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability
作者
关键词
-
出版物
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 98, Issue 1, Pages 202-209
出版商
Elsevier BV
发表日期
2015-12-19
DOI
10.1016/j.ajhg.2015.11.004

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