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Article

Genetics in pulmonary arterial hypertension in a large homogeneous Japanese population.

Clinical genetics - 1 Jul 2018

Gamou S, Kataoka M, Aimi Y, Chiba T, Momose Y, Isobe S, Hirayama T, Yoshino H, Fukuda K, Satoh T

Abstract excerpt

Pulmonary arterial hypertension (PAH) is a rare but serious disease with a grave prognosis. Bone morphogenetic protein type 2 receptor (BMPR2) gene is a strong pathogenic factor for PAH. As a collaborative team from Kyorin University and Keio University in Japan, we have analyzed the BMPR2 gene in 356 probands and more than 50 family members, including secondary patients. Importantly, the study population is a...

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Share to Bone Morphogenetic Protein Receptors, Type II
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Familial Primary Pulmonary Hypertension

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Source

Identifiers

PMID: 29023671
DOI: 10.1111/cge.13154

Genes

BMPR2
PAH

Provenance

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