New CACNA1A deletions are associated to migraine phenotypes

BACKGROUND: Familial hemiplegic migraine type 1 (FHM1) is a form of migraine with aura caused by heterozygous mutations in 4 genes: CACNA1A, ATP1A2, SNC1A and PRRT2, but further heterogeneity is expected. Here have been described clinical and molecular features in patients suffering from migraine wi...

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Detalles Bibliográficos
Autores principales: Grieco, G. S., Gagliardi, S., Ricca, I., Pansarasa, O., Neri, M., Gualandi, F., Nappi, G., Ferlini, A., Cereda, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117225/
https://www.ncbi.nlm.nih.gov/pubmed/30167989
http://dx.doi.org/10.1186/s10194-018-0891-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117225/
https://www.ncbi.nlm.nih.gov/pubmed/30167989
http://dx.doi.org/10.1186/s10194-018-0891-x

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