From bone morphogenic protein receptor II mutations to heritable pulmonary arterial hypertension-the long and winding road

J Heart Lung Transplant. 2017 Feb;36(2):134-135. doi: 10.1016/j.healun.2016.08.002. Epub 2016 Aug 17.

Authors

Barbara C Cahill¹, Nathan D Hatton², John J Ryan³

Affiliations

¹ Division of Respiratory, Critical Care & Occupational Pulmonary Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA. Electronic address: barbara.cahill@hsc.utah.edu.
² Division of Respiratory, Critical Care & Occupational Pulmonary Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.
³ Division of Cardiovascular Medicine, University of Utah School of Medicine, Salt Lake City, Utah, USA.

PMID: 27646063
DOI: 10.1016/j.healun.2016.08.002

No abstract available

Publication types

Editorial
Comment

MeSH terms

Bone Morphogenetic Protein Receptors, Type II / genetics*
Familial Primary Pulmonary Hypertension
Humans
Mutation

Substances

BMPR2 protein, human
Bone Morphogenetic Protein Receptors, Type II