Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an "HHT-like" syndrome in children. (2021)

First Author: Hodgson J
Attributed to:  Mechanisms underlying the development of pulmonary arterial hypertension funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/mgg3.1685

PubMed Identifier: 33834622

Publication URI: http://europepmc.org/abstract/MED/33834622

Type: Journal Article/Review

Volume: 9

Parent Publication: Molecular genetics & genomic medicine

Issue: 12

ISSN: 2324-9269