Mutations of bone morphogenetic protein receptor type II are not found in patients with pulmonary hypertension and underlying connective tissue diseases

This publication has 9 references indexed in Scilit:

• Genetic Clues to the Cause of Primary Pulmonary Hypertension
  New England Journal of Medicine, 2001
• Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia
  New England Journal of Medicine, 2001
• Mutation in the Gene for Bone Morphogenetic Protein Receptor II as a Cause of Primary Pulmonary Hypertension in a Large Kindred
  New England Journal of Medicine, 2001
• BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension
  American Journal of Human Genetics, 2001
• Pulling apart pulmonary hypertension
  Nature Genetics, 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
• The 1982 revised criteria for the classification of systemic lupus erythematosus
  Arthritis & Rheumatism, 1982
• Preliminary criteria for the classification of systemic sclerosis (scleroderma)
  Arthritis & Rheumatism, 1980