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Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. (2018)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1126/scitranslmed.aai7795

PubMed Identifier: 29321258

Publication URI: http://europepmc.org/abstract/MED/29321258

Type: Journal Article/Review

Volume: 10

Parent Publication: Science translational medicine

Issue: 423

ISSN: 1946-6234