Widening phenotypic spectrum of GABBR2 mutation

被引：8

作者：

Samanta, Debopam ^{[1
]}

Zarate, Yuri A. ^{[2
]}

机构：

[1] Univ Arkansas Med Sci, Dept Pediat, Sect Child Neurol, 1 Childrens Way, Little Rock, AR 72202 USA

[2] Univ Arkansas Med Sci, Arkansas Childrens Hosp, Dept Pediat, Sect Genet & Metab, Little Rock, AR 72205 USA

来源：

ACTA NEUROLOGICA BELGICA | 2019年 / 119卷 / 03期

关键词：

GABBR2; Epileptic encephalopathy; Rett-like phenotype; Absence seizure; Intellectual impairment; RETT-SYNDROME;

D O I：

10.1007/s13760-019-01088-5

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：493 / 496

页数：4

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