A unique myopathic phenotype of novel SPTAN1 mutation without encephalopathy in siblings

被引：0
|
作者：
Anilkumar, Arayamparambil [1 ]
Binalsheikh, Ibrahim [1 ]
Miller, Douglas [2 ]
机构：
[1] Dept Child Hlth, Div Pediat Neurol, Columbia, MO USA
[2] Univ Missouri, Dept Pathol & Anat Sci, Columbia, MO USA
来源：
NEUROLOGY | 2019年 / 92卷 / 15期
关键词：
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：
P2.4-042
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页数：2
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