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Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes
BACKGROUND AND AIM: Migraine is the most common neurological disorder, affecting approximately 12 % of the adult population worldwide, caused by both environmental and genetic factors. Three causative genes have been identified in familial hemiplegic migraine (FHM) families: CACNA1A, ATP1A2, and SCN...
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| Publicat a: | Hum Genomics |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4706665/ https://ncbi.nlm.nih.gov/pubmed/26747084 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40246-015-0057-8 |
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