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De novo KCNA2 mutations cause hereditary spastic paraplegia. (2017)

First Author: Manole A

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