The novel p.L1649Q mutation in theSCN1Aepilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies-Reference-Cited by-同舟云学术

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The novel p.L1649Q mutation in theSCN1Aepilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies

Published:2007-05 Issue:5 Volume:28 Page:522-522
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Vanmolkot Kaate R.J.,Babini Elena,de Vries Boukje,Stam Anine H.,Freilinger Tobias,Terwindt Gisela M.,Norris Lisa,Haan Joost,Frants Rune R.,Ramadan Nabih M.,Ferrari Michel D.,Pusch Michael,van den Maagdenberg Arn M.J.M.,Dichgans Martin

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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