A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants

BACKGROUND: Cluster Headache (CH) is a severe primary headache, with a poorly understood pathophysiology. Complex genetic factors are likely to play a role in CH etiology; however, no confirmed gene associations have been identified. The aim of this study is to identify genetic variants influencing...

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Detalles Bibliográficos
Autores principales: Bacchelli, Elena, Cainazzo, Maria Michela, Cameli, Cinzia, Guerzoni, Simona, Martinelli, Angela, Zoli, Michele, Maestrini, Elena, Pini, Luigi Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153392/
https://www.ncbi.nlm.nih.gov/pubmed/27957625
http://dx.doi.org/10.1186/s10194-016-0705-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5153392/
https://www.ncbi.nlm.nih.gov/pubmed/27957625
http://dx.doi.org/10.1186/s10194-016-0705-y

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