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Pulmonary Arterial Hypertension: Insights from Genetic Studies
Familial pulmonary arterial hypertension (FPAH) was described 60 years ago, but real progress in understanding its origins and pathogenesis is just beginning. Germline mutations in bone morphogenetic protein receptor type 2 (BMPR2) are responsible for the disease in most families, and also in many s...
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Thoracic Society
2011
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| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3131832/ https://ncbi.nlm.nih.gov/pubmed/21543793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1513/pats.201007-047MS |
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