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)
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