A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers. (2012)
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/10.1136/jnnp-2012-302402
PubMed Identifier: 22577228
Publication URI: http://europepmc.org/abstract/MED/22577228
Type: Journal Article/Review
Volume: 83
Parent Publication: Journal of neurology, neurosurgery, and psychiatry
Issue: 8
ISSN: 0022-3050