Common genetic variation associated with Mendelian disease severity revealed through cryptic phenotype analysis. (2022)

First Author: Blair DR

Attributed to: UK Biobank (core renewal) funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41467-022-31030-y

PubMed Identifier: 35760791

Publication URI: http://europepmc.org/abstract/MED/35760791

Type: Journal Article/Review

Volume: 13

Parent Publication: Nature communications

Issue: 1

ISSN: 2041-1723