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SIGMAR1 mutation associated with autosomal recessive Silver-like syndrome. (2016)

First Author: Horga A

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/10.1212/wnl.0000000000003212

PubMed Identifier: 27629094

Publication URI: http://europepmc.org/abstract/MED/27629094

Type: Journal Article/Review

Volume: 87

Parent Publication: Neurology

Issue: 15

ISSN: 0028-3878