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

页码：385 / 385

页数：1

共 50 条

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