Compound Heterozygous CACNA1H Mutations Associated with Severe Congenital Amyotrophy

被引：0
|
作者：
McMillan, H.
Carter, M.
Tomin, A.
Weiss, N.
机构：
来源：
ANNALS OF NEUROLOGY | 2019年 / 86卷
关键词：
Neuromuscular Disorders; Rare Diseases; Neonatal Neurology;
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
195
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收藏
页码：S132 / S132
页数：1
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