Article
Recent advances in pulmonary arterial hypertension
2018-07-24
Abstract excerpt
Pulmonary arterial hypertension (PAH) is a rare disorder with a high mortality rate. Treatment options have improved in the last 20 years, but patients still die prematurely of right heart failure. Though rare, it is heterogeneous at the genetic and molecular level, and understanding and exploiting this is key to the development of more effective treatments. BMPR2 , encoding bone morphogenetic receptor type 2, is...
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Identifiers and source
- Literature Corpus work
- 5eb058d7-184b-5c47-84bb-75a5dfd24064
- DOI
- 10.12688/f1000research.14984.1
