Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation. (2017)
Attributed to:
Computational Genomics Analysis and Training programme (CGAT)
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