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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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| 出版年: | BMJ Case Rep |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Publishing Group
2019
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| 主題: | |
| オンライン･アクセス: | 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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