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Novel missense mutation in the ATP1A2 gene associated with atypical sporadic hemiplegic migraine
Hemiplegic migraine (HM) is a rare subtype of migraine with aura in which attacks include transient motor weakness or hemiparesis that can last several days. HM is linked to mutations in three different genes, CACNA1A, ATP1A2 and SCN1A, which encode for ion transporters. The clinical spectrum includ...
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| Publicado no: | BMJ Case Rep |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6781968/ https://ncbi.nlm.nih.gov/pubmed/31586957 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-231129 |
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