Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies

Hemiplegic migraine (HM) is a rare and severe subtype of autosomal dominant migraine, characterized by a complex aura including some degree of motor weakness. Mutations in four genes (CACNA1A, ATP1A2, SCN1A and PRRT2) have been detected in familial and in sporadic cases. This genetically and clinica...

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書誌詳細
主要な著者: Carreño, Oriel, Corominas, Roser, Serra, Selma Angèlica, Sintas, Cèlia, Fernández-Castillo, Noèlia, Vila-Pueyo, Marta, Toma, Claudio, Gené, Gemma G, Pons, Roser, Llaneza, Miguel, Sobrido, María-Jesús, Grinberg, Daniel, Valverde, Miguel Ángel, Fernández-Fernández, José Manuel, Macaya, Alfons, Cormand, Bru
フォーマット: Artigo
言語:Inglês
出版事項: Blackwell Publishing Ltd 2013
主題:
Original Articles
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3865589/
https://ncbi.nlm.nih.gov/pubmed/24498617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.24
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