Divergent sodium channel defects in familial hemiplegic migraine-Reference-Cited by-同舟云学术

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Divergent sodium channel defects in familial hemiplegic migraine

Published:2008-07-09 Issue:28 Volume:105 Page:9799-9804
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Kahlig K. M.,Rhodes T. H.,Pusch M.,Freilinger T.,Pereira-Monteiro J. M.,Ferrari M. D.,van den Maagdenberg A. M. J. M.,Dichgans M.,George A. L.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference41 articles.

2. Migraine: gene mutations and functional consequences

3. A Report on the Journal 2004

4. Increased risk of migraine with typical aura in probands with familial hemiplegic migraine and their relatives

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

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