Evidence for an association between migraine and the hypocretin receptor 1 gene

The aim of our study was to investigate whether genetic variants in the hypocretin receptor 1 (HCRTR1) gene could modify the occurrence and the clinical features of migraine. Using a case–control strategy we genotyped 384 migraine patients and 259 controls for three SNPs in the HCRTR1 gene. Genotypi...

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Detalles Bibliográficos
Autores principales: Rainero, Innocenzo, Rubino, Elisa, Gallone, Salvatore, Fenoglio, Pierpaola, Picci, Luigi Rocco, Giobbe, Laura, Ostacoli, Luca, Pinessi, Lorenzo
Formato: Texto
Lenguaje:English
Publicado: Springer Milan 2011
Materias:
Original
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072499/
https://www.ncbi.nlm.nih.gov/pubmed/21344296
http://dx.doi.org/10.1007/s10194-011-0314-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072499/
https://www.ncbi.nlm.nih.gov/pubmed/21344296
http://dx.doi.org/10.1007/s10194-011-0314-8

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