Strong genetic evidence for association of TOR1A/TOR1B with idiopathic dystonia.
Neurology. 2006 Nov 28;67(10):1857-9
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摘要
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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基因功能
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原始数据
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文献解读
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