📣 Try out the NEW Gateway to Research and let us know what you think.

We're looking for users to test the new service during August and September and share their feedback. Express your interest by completing this short form.

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. (2017)

First Author: Styrkarsdottir U
Attributed to:  Centre for Genomic Research: Genomics Hub Renewal funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.3816

PubMed Identifier: 28319091

Publication URI: http://europepmc.org/abstract/MED/28319091

Type: Journal Article/Review

Volume: 49

Parent Publication: Nature genetics

Issue: 5

ISSN: 1061-4036