Chen, Yongping; Chen, Ke; Burgunder, Jean-Marc; Song, Wei; Huang, Rui; Zhao, Bi; Cao, Bei; Chen, Xueping; Jiang, Yi; Shang, Hui-Fang (2012). Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese population. Journal of the neurological sciences, 323(1-2), pp. 228-31. Amsterdam: Elsevier 10.1016/j.jns.2012.09.025
Full text not available from this repository.The deletion mutation of glutamate codon (GAG) in the TOR1A gene is a major cause of primary generalized dystonia. Recent genetic studies suggest that the rs1182 polymorphism in the same gene may represent a risk factor for primary dystonia. However, this finding has been inconsistent. Furthermore, no data on such an association in a Chinese population have been published.
Item Type: |
Journal Article (Original Article) |
---|---|
Division/Institute: |
04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Neurology |
UniBE Contributor: |
Burgunder, Jean-Marc |
ISSN: |
0022-510X |
Publisher: |
Elsevier |
Language: |
English |
Submitter: |
Factscience Import |
Date Deposited: |
04 Oct 2013 14:39 |
Last Modified: |
05 Dec 2022 14:12 |
Publisher DOI: |
10.1016/j.jns.2012.09.025 |
PubMed ID: |
23058565 |
Web of Science ID: |
000311132700039 |
URI: |
https://boris.unibe.ch/id/eprint/15969 (FactScience: 223492) |