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Genetic association analysis of 77,539 genomes reveals rare disease etiologies. (2023)

First Author: Greene D

Attributed to: Deep phenotyping to improve understanding of causal mechanisms and underlying gene mutations in primary lymphoedema and lymphatic malformations funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41591-023-02211-z

PubMed Identifier: 36928819

Publication URI: http://europepmc.org/abstract/MED/36928819

Type: Journal Article/Review

Volume: 29

Parent Publication: Nature medicine

Issue: 3

ISSN: 1078-8956