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