A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease. (2015)

First Author: Kun-Rodrigues C
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/10.1093/hmg/ddv376

PubMed Identifier: 26362251

Publication URI: http://europepmc.org/abstract/MED/26362251

Type: Journal Article/Review

Volume: 24

Parent Publication: Human molecular genetics

Issue: 23

ISSN: 0964-6906