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Absence of influence of gender and BMPR2 mutation type on clinical phenotypes of pulmonary arterial hypertension

BACKGROUND: Previous studies indicate that patients with pulmonary arterial hypertension (PAH) carrying a mutation in the bone morphogenetic protein receptor type 2 (BMPR2) gene, develop the disease 10 years earlier than non-carriers, and have a more severe hemodynamic compromise at diagnosis. A rec...

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Detalles Bibliográficos
Autores principales: Girerd, Barbara, Montani, David, Eyries, Mélanie, Yaici, Azzedine, Sztrymf, Benjamin, Coulet, Florence, Sitbon, Olivier, Simonneau, Gérald, Soubrier, Florent, Humbert, Marc
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2898773/
https://www.ncbi.nlm.nih.gov/pubmed/20534176
http://dx.doi.org/10.1186/1465-9921-11-73