Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene. (2017)

First Author: Rossor AM

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.nmd.2016.10.001

PubMed Identifier: 27816334

Publication URI: http://europepmc.org/abstract/MED/27816334

Type: Journal Article/Review

Volume: 27

Parent Publication: Neuromuscular disorders : NMD

Issue: 1

ISSN: 0960-8966