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American Association for the Advancement of Science, Science Translational Medicine, 423(10), 2018

DOI: 10.1126/scitranslmed.aai7795

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Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease

This paper is available in a repository.
This paper is available in a repository.

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Abstract

Crohn’s disease (CD)–associated variants in the LRRK2 gene for risk (N2081D) and for protection (N551K) mediate shared effects in CD and Parkinson’s disease.