Novel mutations in the Na+, K+-ATPase pump geneATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions-Reference-Cited by-同舟云学术

Novel mutations in the Na+, K+-ATPase pump geneATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

Published:2003-08-28 Issue:3 Volume:54 Page:360-366
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Vanmolkot Kaate R. J.,Kors Esther E.,Hottenga Jouke-Jan,Terwindt Gisela M.,Haan Joost,Hoefnagels Wil A. J.,Black David F.,Sandkuijl Lodewijk A.,Frants Rune R.,Ferrari Michel D.,Van Den Maagdenberg Arn M. J. M.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference28 articles.

1. Flunarizine in Prophylaxis of Childhood Migraine: A Double-Blind, Placebo-Controlled, Crossover Study

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

3. The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel

4. Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity

5. A new locus for hemiplegic migraine maps to chromosome 1q31

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