Genetic variation of CACNA1H in idiopathic generalized epilepsy

被引:87
作者
Heron, SE [1 ]
Phillips, HA
Mulley, JC
Mazarib, A
Neufeld, MY
Berkovic, SF
Scheffer, IE
机构
[1] Womens & Childrens Hosp, Dept Med Genet, Adelaide, SA, Australia
[2] Royal Childrens Hosp, Dept Neurol, Melbourne, Vic, Australia
[3] Monash Med Ctr, Dept Neurol, Melbourne, Vic, Australia
[4] Univ Melbourne, Austin Hlth, Dept Med Neurol, Parkville, Vic 3052, Australia
[5] Univ Melbourne, Epilepsy Res Ctr, Parkville, Vic 3052, Australia
[6] Tel Aviv Sourasky Med Ctr, Dept Neurol, Tel Aviv, Israel
关键词
D O I
10.1002/ana.20028
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
引用
收藏
页码:595 / 596
页数:2
相关论文
共 3 条
[1]   Association between genetic variation of CACNA1H and childhood absence epilepsy [J].
Chen, YC ;
Lu, JJ ;
Pan, H ;
Zhang, YH ;
Wu, HS ;
Xu, KM ;
Liu, XY ;
Jiang, YW ;
Bao, XH ;
Yao, ZJ ;
Ding, KY ;
Lo, WHY ;
Qiang, BQ ;
Chan, P ;
Shen, Y ;
Wu, XR .
ANNALS OF NEUROLOGY, 2003, 54 (02) :239-243
[2]   Unraveling monogenic channelopathies and their implications for complex polygenic disease [J].
Gargus, JJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (04) :785-803
[3]   Truncation of the GABAA-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus [J].
Harkin, LA ;
Bowser, DN ;
Dibbens, LM ;
Singh, R ;
Phillips, F ;
Wallace, RH ;
Richards, MC ;
Williams, DA ;
Mulley, JC ;
Berkovic, SF ;
Scheffer, IE ;
Petrou, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (02) :530-536