Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families

Mutation analysis of CACNA1A and ATP1A2 genes in Brazilian FHM families

Familial hemiplegic migraine (FHM) is a rare autosomal dominant form of migraine with aura. This disease has been associated with missense mutations in the CACNA1A and ATP1A2 genes. The aim of this study was to identify whether CACNA1A and ATP1A2 are or not related to Brazilian FHM. Here we screened...

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Bibliographic Details
Main Authors: Luciana R. Lopes, Mario Fernando Prieto Peres, Kaate R.J. Vanmolkot, Patrícia R. Tobo, Eliova Zukerman, Rune R. Frants, Arn M.J.M. van den Maagdenberg, Carlos Alberto Moreira-Filho
Format: Article
Language:English
Published: Thieme Revinter Publicações 2006-09-01
Series:Arquivos de Neuro-Psiquiatria
Subjects:
familial hemiplegic migraine
CACNA1A
ATP1A2
SCN1a
gene
mutation
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2006000400001&tlng=en
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