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Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
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2010 (English)In: Lancet Neurology, ISSN 1474-4422, E-ISSN 1474-4465, Vol. 9, no 10, 986-994 p.Article in journal (Refereed) Published
Abstract [en]

We have found strong evidence of a genetic association of two single nucleotide polymorphisms on chromosome 9 with sporadic ALS, in line with findings from previous independent GWAS of ALS and linkage studies of ALS-frontotemporal dementia. Our findings together with these earlier findings suggest that genetic variation at this locus on chromosome 9 causes sporadic ALS and familial ALS-frontotemporal dementia. Resequencing studies and then functional analysis should be done to identify the defective gene.

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2010. Vol. 9, no 10, 986-994 p.
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URN: urn:nbn:se:umu:diva-42297DOI: 10.1016/S1474-4422(10)70197-6ISI: 000283616700013PubMedID: 20801717OAI: oai:DiVA.org:umu-42297DiVA: diva2:409090
Available from: 2011-04-07 Created: 2011-04-07 Last updated: 2017-12-11Bibliographically approved

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