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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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| Yayımlandı: | Semin Respir Crit Care Med |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2017
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| Konular: | |
| Online Erişim: | 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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