De novo KCNA2 mutations cause hereditary spastic paraplegia. (2017)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/ana.24866
PubMed Identifier: 28032718
Publication URI: http://europepmc.org/abstract/MED/28032718
Type: Journal Article/Review
Volume: 81
Parent Publication: Annals of neurology
Issue: 2
ISSN: 0364-5134