Primary pulmonary hypertension may be a heterogeneous disease with a second locus on chromosome 2q31

This publication has 17 references indexed in Scilit:

• Functional analysis of bone morphogenetic protein type II receptor mutations underlying primary pulmonary hypertension
  Human Molecular Genetics, 2002
• Primary Pulmonary Hypertension Is Associated With Reduced Pulmonary Vascular Expression of Type II Bone Morphogenetic Protein Receptor
  Circulation, 2002
• BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension
  American Journal of Human Genetics, 2001
• Sporadic primary pulmonary hypertension is associated with germline mutations of the gene encoding BMPR-II, a receptor member of the TGF-beta family
  Journal of Medical Genetics, 2000
• Abnormal Pulmonary Artery Pressure Response in Asymptomatic Carriers of Primary Pulmonary Hypertension Gene
  Circulation, 2000
• Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension
  Nature Genetics, 2000
• Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene
  American Journal of Human Genetics, 2000
• Fine Mapping of PPH1, a Gene for Familial Primary Pulmonary Hypertension, to a 3-cM Region on Chromosome 2q33
  American Journal of Respiratory and Critical Care Medicine, 2000
• Mapping of Familial Primary Pulmonary Hypertension Locus (PPH1) to Chromosome 2q31-q32
  Circulation, 1997
• Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32
  Nature Genetics, 1997