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Analysis of 200 000 exome-sequenced UK Biobank subjects illustrates the contribution of rare genetic variants to hyperlipidaemia. (2022)

First Author: Curtis D

Attributed to: UCL Biosciences Big Data funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmedgenet-2021-107752

PubMed Identifier: 33910933

Publication URI: http://europepmc.org/abstract/MED/33910933

Type: Journal Article/Review

Volume: 59

Parent Publication: Journal of medical genetics

Issue: 6

ISSN: 0022-2593