A novel GFAP mutation in a type II (late-onset) Alexander disease patient

被引：0
|
作者：
Anderson Rodrigues Brandão de Paiva
Fernando Freua
Leandro Tavares Lucato
Jacy Parmera
Denise Dória
Paulo Ribeiro Nóbrega
Thiago Rosa Olávio
Lúcia Inês Macedo-Souza
Fernando Kok
机构：
[1] Hospital das Clínicas da Universidade de São Paulo,Neurogenetics, Neurology Department
[2] Hospital das Clínicas da Universidade de São Paulo,Radiology Institute
[3] Universidade de São Paulo,Centro de Estudos do Genoma Humano
来源：
Journal of Neurology | 2016年 / 263卷
关键词：
Cerebellar Ataxia; White Matter Hyperintensity; Alexander Disease; Autosomal Dominant Condition; Spastic Gait;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
页码：821 / 822
页数：1
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