Unusual phenotypic expression of the DYT1 mutation
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
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1. The DYT1 phenotype and guidelines for diagnostic testing;Bressman;Neurology,2000
2. Detailed haplotype analysis in Ashkenazi-Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations;Valente;Ann Hum Genet,1999
3. The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews;Kramer;Am J Hum Genet,1994
4. Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium;Ozelius;Genome Res,1997
5. Frequency of the DYT1 mutation in primary torsion dystonia without family history;Brassat;Arch Neurol,2000
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