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Article

Genetics and pharmacogenomics in pulmonary arterial hypertension.

Heart failure clinics - 1 Jul 2012

Smith Benjamin P, Best D Hunter, Elliott C Gregory

Abstract excerpt

Pulmonary arterial hypertension (PAH) is an uncommon disease in the general population, but a disease with significant morbidity and mortality. The prevalence of heritable PAH (HPAH) remains unknown. The reason for incomplete penetrance of HPAH is not well understood. A patient's clinical response to disease-specific therapy is complex, involving the severity of the patient's disease, other comorbidities,...

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Topics

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Share to Anticipation, Genetic
Share to Antigens, CD
Share to Bone Morphogenetic Protein Receptors, Type II

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Hypertension, Pulmonary

Share to Pharmacogenetics

Share to Pulmonary Artery

Share to Receptors, Cell Surface

Source

Identifiers

PMID: 22748897
DOI: 10.1016/j.hfc.2012.04.008

Genes

PAH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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