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A clinical and family history study of Parkinson's disease in heterozygous glucocerebrosidase mutation carriers. (2012)

First Author: McNeill A

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