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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...
Uloženo v:
| Vydáno v: | J Headache Pain |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Milan
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8317284/ https://ncbi.nlm.nih.gov/pubmed/34320921 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s10194-021-01297-5 |
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