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Functional mutations in 5′UTR of the BMPR2 gene identified in Chinese families with pulmonary arterial hypertension
Abstract. Pulmonary arterial hypertension (PAH) is a progressive pulmonary vasculopathy with significant morbidity and mortality. Bone morphogenetic protein receptor type 2 (BMPR2) has been well recognized as the principal gene responsible for heritable and sporadic PAH. Four unrelated Chinese patie...
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| Publicado no: | Pulm Circ |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
University of Chicago Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4860546/ https://ncbi.nlm.nih.gov/pubmed/27162618 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1086/685078 |
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