A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability
出版年份 2018 全文链接
标题
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability
作者
关键词
-
出版物
eLife
Volume 7, Issue -, Pages -
出版商
eLife Sciences Organisation, Ltd.
发表日期
2018-05-22
DOI
10.7554/elife.32451
参考文献
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