An association study of the calcium channel gene CACNA1A and idiopathic generalised epilepsy

被引:0
|
作者
Chioza, BA
Goodwin, HJ
McCormick, D
Blower, J
Nashef, L
Asherson, P
Makoff, AJ
机构
关键词
D O I
暂无
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:A355 / A355
页数:1
相关论文
共 50 条
  • [31] CACNA1A gene mutations in familial hemiplegic migraine
    Arn M.J.M. van den Maagdenberg
    Joerg Striessnig
    Michel D. Ferrari
    Rune R. Frants
    The Journal of Headache and Pain, 2000, 1 (Suppl 2) : S121 - S128
  • [32] Is the CACNA1A gene involved in familial migraine with aura?
    R. Brugnoni
    M. Leone
    A. Rigamonti
    E. Moranduzzo
    F. Cornelio
    R. Mantegazza
    G. Bussone
    Neurological Sciences, 2002, 23 : 1 - 5
  • [33] Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia
    Ducros, A
    Denier, C
    Joutel, A
    Vahedi, K
    Michel, A
    Darcel, F
    Madigand, M
    Guerouaou, D
    Tison, F
    Julien, J
    Hirsch, E
    Chedru, F
    Bisgård, C
    Lucotte, G
    Després, P
    Billard, C
    Barthez, MA
    Ponsot, G
    Bousser, MG
    Tournier-Lasserve, E
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (01) : 89 - 98
  • [34] Genotype-phenotype correlation of CACNA1A variants in children with epilepsy
    Niu, Xueyang
    Yang, Ying
    Chen, Yi
    Cheng, Miaomiao
    Liu, Ming
    Ding, Changhong
    Tian, Xiaojuan
    Yang, Zhixian
    Jiang, Yuwu
    Zhang, Yuehua
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2022, 64 (01): : 105 - 111
  • [35] Correlations of Calcium Voltage-Gated Channel Subunit Alpha1 A (CACNA1A) Gene Polymorphisms with Benign Paroxysmal Positional Vertigo
    Pan, Ruichun
    Qi, Xiaokun
    Wang, Fei
    Chong, Yi
    Li, Xia
    Chen, Qiang
    MEDICAL SCIENCE MONITOR, 2019, 25 : 946 - 951
  • [36] New mutations in the voltage-gated calcium channel gene CACNA1A in british families with episodic ataxia type 2.
    Eunson, LH
    Jouvenceau, A
    Ramesh, V
    Zuberi, SM
    Nairne, A
    Hyman, N
    Wood, NW
    Spauschus, A
    Kullmann, DM
    Hanna, MG
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A293 - A293
  • [37] Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity
    Fletcher, CF
    Tottene, A
    Lennon, VA
    Wilson, SM
    Dubel, SJ
    Paylor, R
    Hosford, DA
    Tessarollo, L
    Tessarollo, L
    McEnery, MW
    Pietrobon, D
    Copeland, NG
    Jenkins, NA
    FASEB JOURNAL, 2001, 15 (07): : 1288 - 1290
  • [38] Penetrance of a new mutant allele of the voltage gated calcium channel gene CACNA1A is dependent on amyloid precursor protein (APP) concentration
    Mellem, JE
    Toxopeus, C
    Stephenson, DA
    Turner, S
    Peterson, D
    Gilchrist, J
    Carlson, GA
    NEUROBIOLOGY OF AGING, 2004, 25 : S228 - S228
  • [39] Identification of four novel nonsense mutations in the CACNA1A gene
    Mariotti, C
    Romano, S
    Gellera, C
    Castellotti, B
    Passariello, P
    Testa, D
    Fancellu, R
    Salmaggi, A
    Di Donato, S
    JOURNAL OF NEUROLOGY, 2005, 252 : 85 - 85
  • [40] Is benign paroxysmal torticollis related to mutations in the CACNA1A gene?
    Douglass, Laurie M.
    Rosman, N. Paul
    Milunsky, Jeff M.
    NEUROLOGY, 2007, 68 (12) : A47 - A47