Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort

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

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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:

17 Mar 2015 21:33

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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