Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation
出版年份 2014 全文链接
标题
Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation
作者
关键词
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出版物
HUMAN MOLECULAR GENETICS
Volume 23, Issue 13, Pages 3481-3489
出版商
Oxford University Press (OUP)
发表日期
2014-02-06
DOI
10.1093/hmg/ddu056
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