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Article

The genetics of pulmonary arterial hypertension.

Circulation research - 20 Jun 2014

Austin Eric D, Loyd James E

Abstract excerpt

Pulmonary arterial hypertension (PAH) is a progressive and fatal disease for which there is an ever-expanding body of genetic and related pathophysiological information on disease pathogenesis. Many germline gene mutations have now been described, including mutations in the gene coding bone morphogenic protein receptor type 2 (BMPR2) and related genes. Recent advanced gene-sequencing methods have facilitated the...

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Topics

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Share to Bone Morphogenetic Protein Receptors, Type II
Share to Caveolin 1
Share to Epigenesis, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Familial Primary Pulmonary Hypertension

Share to Gonadal Steroid Hormones

Share to Hypertension, Pulmonary

Share to Potassium Channels, Tandem Pore Domain

Share to Protein Precursors

Source

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Identifiers

PMID: 24951767
DOI: 10.1161/CIRCRESAHA.115.303404
PMCID: PMC4137413

Genes

PAH
BMPR2
CAV1
KCNK3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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