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Authors
Clarimon, JordiAsgeirsson, Hilmir
Singleton, Andrew
Jakobsson, Finnbogi
Hjaltason, Haukur
Hardy, John
Sveinbjornsdottir, Sigurlaug
Issue Date
2005-05-01
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Ann. Neurol. 2005, 57(5):765-7Abstract
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.Description
To access publisher full text version of this article. Please click on the hyperlink in Additional Links fieldAdditional Links
http://dx.doi.org/10.1002/ana.20485ae974a485f413a2113503eed53cd6c53
10.1002/ana.20485
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