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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Detalles Bibliográficos
Autores principales: Pfarr, Nicole, Szamalek-Hoegel, Justyna, Fischer, Christine, Hinderhofer, Katrin, Nagel, Christian, Ehlken, Nicola, Tiede, Henning, Olschewski, Horst, Reichenberger, Frank, Ghofrani, Ardeschir HA, Seeger, Werner, Grünig, Ekkehard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3163544/
https://www.ncbi.nlm.nih.gov/pubmed/21801371
http://dx.doi.org/10.1186/1465-9921-12-99

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