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Erratum to: Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation. (2015)

First Author: Koutsis G

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/s00415-015-7846-9

PubMed Identifier: 26162716

Publication URI: http://europepmc.org/abstract/MED/26162716

Type: Journal Article/Review

Volume: 262

Parent Publication: Journal of neurology

Issue: 8

ISSN: 0340-5354