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Homozygous mutation in HSPB1 causing distal vacuolar myopathy and motor neuropathy. (2017)

First Author: Bugiardini E

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/nxg.0000000000000168

PubMed Identifier: 28702508

Publication URI: http://europepmc.org/abstract/MED/28702508

Type: Journal Article/Review

Volume: 3

Parent Publication: Neurology. Genetics

Issue: 4

ISSN: 2376-7839