A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome

Despite recent progress in the characterization of genetic loci associated with multiple sclerosis (MS) risk, the ubiquitous linkage disequilibrium operating across the genome has stalled efforts to distinguish causative variants from proxy single-nucleotide polymorphisms (SNPs). Here, we have ident...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Didonna, Alessandro, Isobe, Noriko, Caillier, Stacy J., Li, Kathy H., Burlingame, Alma L., Hauser, Stephen L., Baranzini, Sergio E., Patsopoulos, Nikolaos A., Oksenberg, Jorge R.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2015
Assuntos:
Association Studies Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5007634/
https://ncbi.nlm.nih.gov/pubmed/26433934
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv412
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