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Multiple system atrophy and repeat expansions in C9orf72. (2014)

First Author: Schottlaender LV

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/10.1001/jamaneurol.2014.1808

PubMed Identifier: 25200542

Publication URI: http://europepmc.org/abstract/MED/25200542

Type: Journal Article/Review

Volume: 71

Parent Publication: JAMA neurology

Issue: 9

ISSN: 2168-6149