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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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Bibliografske podrobnosti
izdano v:Semin Respir Crit Care Med
Main Authors: Chew, Joshua D., Loyd, James E., Austin, Eric D.
Format: Artigo
Jezik:Inglês
Izdano: 2017
Teme:
Online dostop: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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