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Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia. | LitMetric
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Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.

C Kamm F Asmus J Mueller P Mayer M Sharma U J Muller S Beckert R Ehling T Illig H E Wichmann W Poewe J C Mueller T Gasser

Neurology

Department of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tuebingen, Hoppe-Seyler-Str. 3, 72086 Tuebingen, Germany.

Published: November 2006

Recently, association of a TOR1A(DYT1)/TOR1B risk haplotype with common forms of idiopathic dystonia has been reported in the Icelandic population. Here we report a strong association of two single nucleotide polymorphisms within or in close proximity to the TOR1A 3'UTR, with the lowest p value being 0.000008, in a larger cohort of German and Austrian patients with predominantly focal sporadic dystonia.

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http://dx.doi.org/10.1212/01.wnl.0000244423.63406.17DOI Listing

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