Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia
Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia
About this item
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Author / Creator
Publisher
Berlin/Heidelberg: Springer-Verlag
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer-Verlag
Subjects
More information
Scope and Contents
Contents
Primary dystonia (PrD) is characterized by sustained muscle contractions, causing twisting and repetitive movements and abnormal postures. Besides DYT1/
TOR1A
gene, DYT6/
THAP1
gene is the second gene known to cause primary pure dystonia. We screened 281 Serbian primary dystonia patients and 106 neurologically healthy control individual...
Alternative Titles
Full title
Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia
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Record Identifier
TN_cdi_proquest_miscellaneous_1348488036
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1348488036
Other Identifiers
ISSN
0340-5354
E-ISSN
1432-1459
DOI
10.1007/s00415-012-6753-6
