Chen, Y; Burgunder, J-M; Song, W; Huang, R; Shang, H-F (2012). Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort. European journal of neurology, 19(6), pp. 924-6. Oxford: Blackwell Science 10.1111/j.1468-1331.2011.03582.x
Full text not available from this repository. (Request a copy)The D216H single-nucleotide polymorphism (SNP) (rs1801968) in DYT1 exon 4 has been suggested to be a genetic modifier in primary dystonia.
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: |
1351-5101 |
Publisher: |
Blackwell Science |
Language: |
English |
Submitter: |
Factscience Import |
Date Deposited: |
04 Oct 2013 14:39 |
Last Modified: |
05 Dec 2022 14:12 |
Publisher DOI: |
10.1111/j.1468-1331.2011.03582.x |
PubMed ID: |
22054283 |
Web of Science ID: |
000303911600025 |
URI: |
https://boris.unibe.ch/id/eprint/15972 (FactScience: 223495) |
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