Charcot-Marie-Tooth disease type 2CC due to NEFH variants causes a progressive, non-length-dependent, motor-predominant phenotype. (2022)
Attributed to:
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/jnnp-2021-327186
PubMed Identifier: 34518334
Publication URI: http://europepmc.org/abstract/MED/34518334
Type: Journal Article/Review
Volume: 93
Parent Publication: Journal of neurology, neurosurgery, and psychiatry
Issue: 1
ISSN: 0022-3050