Torsin A haplotype predisposes to idiopathic dystonia.
case_control · Level III
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- Record sourced from PubMed, PMID 15852391.
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Abstract
Previous work has suggested that in many neurological diseases genetic variability in the loci predisposing subjects to autosomal dominant disease contributes to the risk of sporadic disease. Here, using a population-based sample of dystonia cases, we show an association with the torsin A haplotype and sporadic idiopathic dystonia.
Medical subject headings
- Dystonia
- Molecular Chaperones