Severe neurodevelopmental disorder with intractable seizures due to a novel SLC1A4 homozygous mutation

被引：0
|
作者：
Sedlackova, L. [1 ,2 ]
Sterbova, K. [2 ,3 ]
Vlckova, M. [2 ,4 ]
Lassuthova, P. [1 ,2 ]
Seeman, P. [1 ,2 ]
机构：
[1] Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, DNA Lab, Prague, Czech Republic
[2] Univ Hosp Motol, Prague, Czech Republic
[3] Charles Univ Prague, Fac Med 2, Dept Pediat Neurol, Prague, Czech Republic
[4] Charles Univ Prague, Fac Med 2, Dept Biol & Med Genet, Prague, Czech Republic
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P09.110A
引用
收藏
页码：1462 / 1463
页数：2
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