Analysis of rare coding variants in 200,000 exome-sequenced subjects reveals novel genetic risk factors for type 2 diabetes. (2022)
Attributed to:
UCL Biosciences Big Data
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/dmrr.3482
PubMed Identifier: 34216101
Publication URI: http://europepmc.org/abstract/MED/34216101
Type: Journal Article/Review
Volume: 38
Parent Publication: Diabetes/metabolism research and reviews
Issue: 1
ISSN: 1520-7552