Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation. (2017)

First Author: Jaffer F
Attributed to:  MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/NXG.0000000000000145

PubMed Identifier: 28382329

Publication URI: http://europepmc.org/abstract/MED/28382329

Type: Journal Article/Review

Volume: 3

Parent Publication: Neurology. Genetics

Issue: 2

ISSN: 2376-7839