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Genetics of Pulmonary Arterial Hypertension
Tremendous progress has been made in understanding the genetics of pulmonary arterial hypertension (PAH) since its description in the 1950s as a primary disorder of the pulmonary vasculature. Heterozygous germline mutations in the gene coding bone morphogenetic receptor type 2 (BMPR2) are detectable...
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| Publicat a: | Semin Respir Crit Care Med |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7722263/ https://ncbi.nlm.nih.gov/pubmed/29032562 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0037-1606201 |
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