CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report

BACKGROUND AND AIMS: Hemiplegic migraine (HM) is a rare form of migraine characterized by the presence of a motor and other types of aura. HM can be sporadic or familial. Familial hemiplegic migraine (FHM) is an autosomal dominant disorder, classified into 3 subtypes, based on the gene involved (CAC...

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Detalles Bibliográficos
Autores principales: Romozzi, Marina, Primiano, Guido, Rollo, Eleonora, Travaglini, Lorena, Calabresi, Paolo, Servidei, Serenella, Vollono, Catello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317284/
https://www.ncbi.nlm.nih.gov/pubmed/34320921
http://dx.doi.org/10.1186/s10194-021-01297-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8317284/
https://www.ncbi.nlm.nih.gov/pubmed/34320921
http://dx.doi.org/10.1186/s10194-021-01297-5

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