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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Detalhes bibliográficos
Publicado no:Neurogenetics
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2020
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7283211/
https://ncbi.nlm.nih.gov/pubmed/32076896
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-020-00606-5
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