Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. (2018)
Attributed to:
Identification and characterisation of causal molecules for Crohn's disease and ulcerative colitis
funded by
MRC
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