Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity. (2013)
Attributed to:
A systematic investigation into the pathogenesis and course of Parkinson's syndrome
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2012.12.012
PubMed Identifier: 23332917
Publication URI: http://europepmc.org/abstract/MED/23332917
Type: Journal Article/Review
Volume: 92
Parent Publication: American journal of human genetics
Issue: 2
ISSN: 0002-9297