Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease. (2018)

First Author: Blauwendraat C
Attributed to:  Molecular Genetic Studies of Schizophrenia funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1001/jamaneurol.2018.1885

PubMed Identifier: 30039155

Publication URI: http://europepmc.org/abstract/MED/30039155

Type: Journal Article/Review

Volume: 75

Parent Publication: JAMA neurology

Issue: 11

ISSN: 2168-6149