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Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.

van Es, Michael A (author)
van Vught, Paul W J (author)
Blauw, Hylke M (author)
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Franke, Lude (author)
Saris, Christiaan G J (author)
Van den Bosch, Ludo (author)
de Jong, Sonja W (author)
de Jong, Vianney (author)
Baas, Frank (author)
van't Slot, Ruben (author)
Lemmens, Robin (author)
Schelhaas, Helenius J (author)
Birve, Anna (author)
Umeå universitet,Neurologi
Sleegers, Kristel (author)
Van Broeckhoven, Christine (author)
Schymick, Jennifer C (author)
Traynor, Bryan J (author)
Wokke, John H J (author)
Wijmenga, Cisca (author)
Robberecht, Wim (author)
Andersen, Peter M (author)
Umeå universitet,Neurologi
Veldink, Jan H (author)
Ophoff, Roel A (author)
van den Berg, Leonard H (author)
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 (creator_code:org_t)
2007-12-16
2008
English.
In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 40:1, s. 29-31
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • We identified a SNP in the DPP6 gene that is consistently strongly associated with susceptibility to amyotrophic lateral sclerosis (ALS) in different populations of European ancestry, with an overall P value of 5.04 x 10(-8) in 1,767 cases and 1,916 healthy controls and with an odds ratio of 1.30 (95% confidence interval (CI) of 1.18-1.43). Our finding is the first report of a genome-wide significant association with sporadic ALS and may be a target for future functional studies.

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