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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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| Publicado no: | J Headache Pain |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Milan
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6117225/ https://ncbi.nlm.nih.gov/pubmed/30167989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s10194-018-0891-x |
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