Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease. (2022)

First Author: Zhu W

Attributed to: UK Biobank (core renewal) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awab456

PubMed Identifier: 35640906

Publication URI: http://europepmc.org/abstract/MED/35640906

Type: Journal Article/Review

Volume: 145

Parent Publication: Brain : a journal of neurology

Issue: 6

ISSN: 0006-8950