Chromosome 9p21 in Amyotrophic Lateral Sclerosis in Finland: A Genome-Wide Association Study

INTRODUCTION: The genetic etiology of amyotrophic lateral sclerosis (ALS) is not well understood. Finland is a well-suited location for a genome-wide association study of ALS, as the incidence of the disease is one of the highest in the world, and because the genetic homogeneity of the Finnish popul...

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Detalhes bibliográficos
Main Authors: Laaksovirta, Hannu, Peuralinna, Terhi, Schymick, Jennifer C., Scholz, Sonja W., Lai, Shaoi-Lin, Myllykangas, Liisa, Sulkava, Raimo, Jansson, Lilja, Hernandez, Dena G., Gibbs, J. Raphael, Nalls, Michael A., Heckerman, David, Tienari, Pentti J., Traynor, Bryan J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2965392/
https://ncbi.nlm.nih.gov/pubmed/20801718
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1474-4422(10)70184-8
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