Toggle Main Menu Toggle Search

Open Access padlockePrints

The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Molecular Epidemiology of Spinocerebellar Ataxia Type 6

Lookup NU author(s): Kate Craig, Sharon Foster, Dr Ann Curtis, Professor Patrick Chinnery

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.

Abstract

We performed a population-based clinical and molecular genetic study of spinocerebellar ataxia type 6 (SCA6) in the northeast of England. The minimum point prevalence of SCA6 was 1.59 in 100,000 (95% confidence interval [CI], 1.04-2.14), and the number of individuals who either had SCA6 or are at risk of developing SCA6 was at least 5.21 in 100,000 (95% CI, 4.31-6.10), or 1 in 19,210. Microsatellite analysis of the CACNA1A gene indicated a founder effect for SCA6 within this region.

Publication metadata

Author(s): Craig K, Keers SM, Archibald K, Curtis A, Chinnery PF

Publication type: Article

Publication status: Published

Journal: Annals of Neurology

Year: 2004

Volume: 55

Issue: 5

Pages: 752-755

ISSN (print): 0364-5134

ISSN (electronic): 1531-8249

Publisher: John Wiley & Sons, Inc.

URL: http://dx.doi.org/10.1002/ana.20110

DOI: 10.1002/ana.20110

PubMed id: 15122720

Altmetrics

Altmetrics provided by Altmetric

Share