Mosaicism of de novo SCN1A mutations in epilepsy: an explanation for variable phenotypes?

被引：0
|
作者：
De lange, I. M. [1 ]
Koudijs, M. [1 ]
van't Slot, R. [1 ]
Mulder, F. [1 ]
Carbo, E. C. [1 ,2 ]
van Kempen, M. [1 ]
Gunning, B. [3 ]
van Gemert, L. [4 ]
Sonsma, A. [1 ]
Savelberg, S. [1 ]
Knoers, N. [1 ]
Brilstra, E. [1 ]
Koeleman, B. [1 ]
机构：
[1] Univ Med Ctr Utrecht, Dept Genet, Ctr Mol Med, Utrecht, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[3] Stichting Epilepsie Instellingen Nederland, Zwolle, Netherlands
[4] Epilepsy Ctr Kempenhaeghe, Heeze, Netherlands
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：
P09.078B
引用
收藏
页码：398 / 398
页数：1
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