Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation

被引：0
|
作者：
Debopam Samanta
机构：
[1] University of Arkansas for Medical Sciences,Division of Child Neurology
来源：
Acta Neurologica Belgica | 2016年 / 116卷
关键词：
KRAS Mutation; Noonan Syndrome; Severe Developmental Delay; SOS1 Gene; Costello Syndrome;
D O I：
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摘要：
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页码：223 / 224
页数：1
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