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/10.17863/cam.79486

Publication URI: https://www.repository.cam.ac.uk/handle/1810/332039

Type: Journal Article/Review