Association between the α1a calcium channel gene CACNA1A and idiopathic generalized epilepsy

被引：77

作者：

Chioza, B

Wilkie, H

Nashef, L

Blower, J

McCormick, D

Sham, P

Asherson, P

Makoff, AJ

机构：

[1] Inst Psychiat, Dept Psychol Med, London SE5 8AF, England

[2] Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London SE5 8AF, England

[3] Kent & Canterbury Hosp, Dept Paediat, Canterbury, Kent, England

[4] Kings Coll London Hosp, Dept Neurol, London SE5 8RX, England

来源：

关键词：

D O I：

10.1212/WNL.56.9.1245

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

[No abstract available]

引用

页码：1245 / 1246

页数：2

共 8 条

[1] A look at linkage disequilibrium
Boehnke, M
[J]. NATURE GENETICS, 2000, 25 (03) : 246 - 247
[2] EXOCYTOTIC CA2+ CHANNELS IN MAMMALIAN CENTRAL NEURONS
DUNLAP, K
LUEBKE, JI
TURNER, TJ
[J]. TRENDS IN NEUROSCIENCES, 1995, 18 (02) : 89 - 98
[3] Absence epilepsy in tottering mutant mice is associated with calcium channel defects
Fletcher, CF
Lutz, CM
OSullivan, TN
Shaughnessy, JD
Hawkes, R
Frankel, WN
Copeland, NG
Jenkins, NA
[J]. CELL, 1996, 87 (04) : 607 - 617
[4] Kendler KS, 1999, AM J MED GENET, V88, P29, DOI 10.1002/(SICI)1096-8628(19990205)88:1<29::AID-AJMG5>3.0.CO
[5] 2-7
[6] Prospects for whole-genome linkage disequilibrium mapping of common disease genes
Kruglyak, L
[J]. NATURE GENETICS, 1999, 22 (02) : 139 - 144
[7] Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
Ophoff, RA
Terwindt, GM
Vergouwe, MN
vanEijk, R
Oefner, PJ
Hoffman, SMG
Lamerdin, JE
Mohrenweiser, HW
Bulman, DE
Ferrari, M
Haan, J
Lindhout, D
vanOmmen, GJB
Hofker, MH
Ferrari, MD
Frants, RR
[J]. CELL, 1996, 87 (03) : 543 - 552
[8] The gene encoding the α1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy
Sander, T
Peters, C
Janz, D
Bianchi, A
Bauer, G
Wienker, TF
Hildmann, T
Epplen, JT
Riess, O
[J]. EPILEPSY RESEARCH, 1998, 29 (02) : 115 - 122