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- W2146852770 endingPage "114" @default.
- W2146852770 startingPage "101" @default.
- W2146852770 abstract "Pulmonary arterial hypertension (PAH) remains a vexing clinical disease with no cure. Despite advances and the discovery of a gene (BMPR2) associated with many of the hereditary forms of the disease, and some cases not previously known to be inherited, the reasons for mutations in this gene as a cause remain somewhat elusive. Clearly, a complex interplay exists between genetic alterations, environmental exposures (including infections), and disease development. This article addresses the advances in the genetics of PAH, including the identification of genetic etiologies and modulators, and the role of genetics in predicting disease progression and targeting therapeutics." @default.
- W2146852770 created "2016-06-24" @default.
- W2146852770 creator A5010401935 @default.
- W2146852770 creator A5054202326 @default.
- W2146852770 creator A5062547544 @default.
- W2146852770 date "2010-01-01" @default.
- W2146852770 modified "2023-09-23" @default.
- W2146852770 title "Genomics of Pulmonary Arterial Hypertension: Implications for Therapy" @default.
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