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A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
Identification of mutations at familial loci for amyotrophic lateral sclerosis (ALS) has provided novel insights into the aetiology of this rapidly progressing fatal neurodegenerative disease. However, genome-wide association studies (GWAS) of the more common (∼90%) sporadic form have been less succ...
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Formaat: | Artigo |
Taal: | Inglês |
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Oxford University Press
2014
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Onderwerpen: | |
Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3959809/ https://ncbi.nlm.nih.gov/pubmed/24256812 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt587 |
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