Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations
BACKGROUND: Mutations in the bone morphogenetic protein receptor 2 (BMPR2) gene can lead to idiopathic pulmonary arterial hypertension (IPAH). This study prospectively screened for BMPR2 mutations in a large cohort of PAH-patients and compared clinical features between BMPR2 mutation carriers and no...
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| Main Authors: | , , , , , , , , , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
29 July 2011
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| In: |
Respiratory research
Year: 2011, Volume: 12, Issue: 1, Pages: 1-10 |
| ISSN: | 1465-993X |
| DOI: | 10.1186/1465-9921-12-99 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1186/1465-9921-12-99 |
| Author Notes: | Nicole Pfarr, Justyna Szamalek-Hoegel, Christine Fischer, Katrin Hinderhofer, Christian Nagel, Nicola Ehlken, Henning Tiede, Horst Olschewski, Frank Reichenberger, Ardeschir H. A. Ghofrani, Werner Seeger and Ekkehard Grünig |
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Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations
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