The Role of Copy Number Variation in Susceptibility to Amyotrophic Lateral Sclerosis: Genome-Wide Association Study and Comparison with Published Loci

BACKGROUND: The genetic contribution to sporadic amyotrophic lateral sclerosis (ALS) has not been fully elucidated. There are increasing efforts to characterise the role of copy number variants (CNVs) in human diseases; two previous studies concluded that CNVs may influence risk of sporadic ALS, wit...

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Detalles Bibliográficos
Autores principales: Wain, Louise V., Pedroso, Inti, Landers, John E., Breen, Gerome, Shaw, Christopher E., Leigh, P. Nigel, Brown, Robert H., Tobin, Martin D., Al-Chalabi, Ammar
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780722/
https://www.ncbi.nlm.nih.gov/pubmed/19997636
http://dx.doi.org/10.1371/journal.pone.0008175

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2780722/
https://www.ncbi.nlm.nih.gov/pubmed/19997636
http://dx.doi.org/10.1371/journal.pone.0008175

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