Identities and frequencies of BMPR2 mutations in Chinese patients with idiopathic pulmonary arterial hypertension
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01335.x/fullpdf
Reference13 articles.
1. Primary pulmonary hypertension;Rubin;N Engl J Med,1997
2. Familial primary pulmonary hypertension (gene PPH1) is caused by mutations in the bone morphogenetic protein receptor-II gene;Deng;Am J Hum Genet,2000
3. Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension;Lane;Nat Genet,2000
4. Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia;Trembath;N Engl J Med,2001
5. Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension;Chaouat;Thorax,2004
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