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Genetics of pulmonary arterial hypertension: do the molecular findings have translational value?
Pulmonary arterial hypertension (PAH) is usually a devastating condition with a poor prognosis. Nearly 10 years ago, the underlying molecular basis of heritable PAH was elucidated with the identification of mutations in the gene encoding the bone morphogenetic protein type II receptor (BMPR-II). Thi...
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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Faculty of 1000 Ltd
2010
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2948374/ https://ncbi.nlm.nih.gov/pubmed/20948811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3410/B2-22 |
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