SPG7 mutations are a common cause of undiagnosed ataxia. (2015)
Attributed to:
COMPUTATIONAL GENOMICS ANALYSIS AND TRAINING (CGAT)AT THE MRC FUNCTIONAL GENOMICS UNIT
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1212/wnl.0000000000001369
PubMed Identifier: 25681447
Publication URI: http://europepmc.org/abstract/MED/25681447
Type: Journal Article/Review
Volume: 84
Parent Publication: Neurology
Issue: 11
ISSN: 0028-3878