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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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| Formato: | Texto |
| Lenguaje: | English |
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Faculty of 1000 Ltd
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948374/ https://www.ncbi.nlm.nih.gov/pubmed/20948811 http://dx.doi.org/10.3410/B2-22 |