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Document type:
Journal Article; Research Support, Non-U.S. Gov't
Author(s):
Kamm, C; Asmus, F; Mueller, J; Mayer, P; Sharma, M; Muller, UJ; Beckert, S; Ehling, R; Illig, T; Wichmann, HE; Poewe, W; Mueller, JC; Gasser, T
Title:
Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.
Abstract:
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.
Journal title abbreviation:
Neurology
Year:
2006
Journal volume:
67
Journal issue:
10
Pages contribution:
1857-9
Language:
eng
Fulltext / DOI:
doi:10.1212/01.wnl.0000244423.63406.17
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/17130424
Print-ISSN:
0028-3878
TUM Institution:
Klinik und Poliklinik für Psychiatrie und Psychotherapie
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