CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report
Abstract 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 invol...
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| Автори: | , , , , , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
BMC
2021-07-01
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| Серія: | The Journal of Headache and Pain |
| Предмети: | |
| Онлайн доступ: | https://doi.org/10.1186/s10194-021-01297-5 |
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