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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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Literature Corpus work
5eb058d7-184b-5c47-84bb-75a5dfd24064
DOI
10.12688/f1000research.14984.1
Open publication

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Recent advances in pulmonary arterial hypertensionDOI 10.12688/f1000research.14984.1
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