A high-density association screen of 155 ion transport genes for involvement with common migraine-Reference-Cited by-同舟云学术

A high-density association screen of 155 ion transport genes for involvement with common migraine

Published:2008-08-02 Issue:21 Volume:17 Page:3318-3331
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Nyholt Dale R.,LaForge K. Steven,Kallela Mikko,Alakurtti Kirsi,Anttila Verneri,Färkkilä Markus,Hämaläinen Eija,Kaprio Jaakko,Kaunisto Mari A.,Heath Andrew C.,Montgomery Grant W.,Göbel Hartmut,Todt Unda,Ferrari Michel D.,Launer Lenore J.,Frants Rune R.,Terwindt Gisela M.,de Vries Boukje,Verschuren W.M. Monique,Brand Jan,Freilinger Tobias,Pfaffenrath Volker,Straube Andreas,Ballinger Dennis G.,Zhan Yiping,Daly Mark J.,Cox David R.,Dichgans Martin,van den Maagdenberg Arn M.J.M.,Kubisch Christian,Martin Nicholas G.,Wessman Maija,Peltonen Leena,Palotie Aarno

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/17/21/3318/17245560/ddn227.pdf

Reference55 articles.

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2. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2;De Fusco;Nat. Genet.,2003

3. Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine;Dichgans;Lancet,2005

4. Deciphering migraine mechanisms: clues from familial hemiplegic migraine genotypes;Moskowitz;Ann. Neurol.,2004

5. Neurobiology of migraine;Pietrobon;Nat. Rev. Neurosci.,2005

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