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De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
Abstract 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 dis...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2017-06-01
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| Colecção: | The Journal of Headache and Pain |
| Assuntos: | |
| Acesso em linha: | http://link.springer.com/article/10.1186/s10194-017-0770-x |
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