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De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
BACKGROUND: Sporadic Hemiplegic Migraine is a rare form of migraine headache. Mutations in three different genes, two ion-channel genes and one encoding an ATP exchanger, CACNA1A, ATP1A2 and SCN1A are all responsible for the FHM phenotype, thus indicating a genetic heterogeneity for this disorder. H...
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| 出版年: | J Headache Pain |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer Milan
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5462664/ https://ncbi.nlm.nih.gov/pubmed/28593511 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s10194-017-0770-x |
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