Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4-Reference-Cited by-同舟云学术

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Published:1996-11 Issue:3 Volume:87 Page:543-552
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Ophoff Roel A,Terwindt Gisela M,Vergouwe Monique N,van Eijk Ronald,Oefner Peter J,Hoffman Susan M.G,Lamerdin Jane E,Mohrenweiser Harvey W,Bulman Dennis E,Ferrari Maurizio,Haan Joost,Lindhout Dick,van Ommen Gert-Jan B,Hofker Marten H,Ferrari Michel D,Frants Rune R

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference49 articles.

1. Calcium antogonist properties of magnesium;Altura;Magnesium,1985

2. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1;Browne;Nat. Genet.,1994

3. Exon amplification;Buckler;Proc. Natl. Acad. Sci. USA,1991

4. The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel;Campbell;Trends Neurosci.,1988

5. Ion-channel defects and aberrant excitability in myotonia and periodic paralysis;Cannon;Trends Neurosci.,1996

Cited by 2098 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Torsional saccadic palsy in episodic ataxia type 2;Journal of Neurology;2024-09-06

2. The Spectrum of Self-Limited Infantile Epilepsy Syndromes;Journal of Pediatric Epilepsy;2024-09-05

3. Natural history of non-polyglutamine CACNA1A disease in Austria;Journal of Neurology;2024-08-07

4. Voltage-gated Calcium Channels as Potential Therapeutic Targets in Migraine;The Journal of Pain;2024-08

5. A Longitudinal Exploration ofCACNA1A-related Hemiplegic Migraine in Children;2024-06-15