Improving interpretation of the clinical significance of SCN1A variants in patients with Dravet syndrome using in silico analysis of missense mutations

被引：0
|
作者：
Gonsales, M. C. [1 ]
Montenegro, M. A. [2 ]
Preto, P. [2 ]
Guerreiro, M. M. [2 ]
Coan, A. C. [2 ]
Quast, M. P. [3 ]
Carvalho, B. S. [3 ]
Lopes-Cendes, I. [1 ]
机构：
[1] Univ Estadual Campinas, Dept Med Genet, Campinas, SP, Brazil
[2] Univ Estadual Campinas, Dept Neurol, Campinas, SP, Brazil
[3] Univ Estadual Campinas, Dept Stat, Campinas, SP, Brazil
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2018年 / 26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：
P09.052D
引用
收藏
页码：385 / 385
页数：1
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