A novel BMPR2 mutation with widely disparate heritable pulmonary arterial hypertension clinical phenotype

Keyphrases

• Clinical Phenotype 100%
• Bone Morphogenetic Protein Receptor 100%
• Heritable Pulmonary Arterial Hypertension 100%
• Pulmonary Arterial Hypertension 66%
• Pulmonary Vascular 33%
• Venules 33%
• Clinical Features 33%
• Capillary 33%
• Venous Disease 33%
• Aggressive Disease 33%
• Variable Phenotype 33%
• α-kinase 33%
• Pulmonary Capillary Hemangiomatosis 33%
• Eukaryotic Translation Initiation Factor 2α 33%
• Novel Pathogenic mutation 33%

Medicine and Dentistry

• Pulmonary Hypertension 100%
• Bone Morphogenetic Protein Receptor 2 100%
• Diseases 20%
• Venule 20%
• Phosphotransferase 20%
• Capillary 20%
• Clinical Feature 20%
• Pulmonary Veno Occlusive Disease 20%
• Pulmonary Capillary Hemangiomatosis 20%
• Initiation Factor 2alpha 20%
• Initiation Factor 20%

Biochemistry, Genetics and Molecular Biology

• Bone Morphogenetic Protein Receptor Type 2 100%
• Phosphotransferase 33%
• Kinase 33%
• Initiation Factor 33%
• Eukaryotic Translation 33%