Familial analysis reveals rare risk variants for migraine in regulatory regions

The most recent genome-wide association study of migraine increased the total number of known migraine risk loci to 38. Still, most of the heritability of migraine remains unexplained, and it has been suggested that rare gene dysregulatory variants play an important role in migraine etiology. Addres...

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Detalles Bibliográficos
Autores principales: Techlo, Tanya Ramdal, Rasmussen, Andreas Høiberg, Møller, Peter L., Bøttcher, Morten, Winther, Simon, Davidsson, Olafur B., Olofsson, Isa A., Chalmer, Mona Ameri, Kogelman, Lisette J. A., Nyegaard, Mette, Olesen, Jes, Hansen, Thomas Folkmann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283211/
https://www.ncbi.nlm.nih.gov/pubmed/32076896
http://dx.doi.org/10.1007/s10048-020-00606-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7283211/
https://www.ncbi.nlm.nih.gov/pubmed/32076896
http://dx.doi.org/10.1007/s10048-020-00606-5

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