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The frequency of spinocerebellar ataxia type 23 in a UK population (2012)

First Author: Fawcett K

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1007/s00415-012-6721-1

PubMed Identifier: 23108490

Publication URI: http://europepmc.org/abstract/MED/23108490

Type: Journal Article/Review

Parent Publication: Journal of Neurology

Issue: 3

ISSN: 0340-5354