Pulmonary artery hypertension in childhood: The transforming growth factor-β superfamily-related genes
Pulmonary artery hypertension (PAH) is very rare in childhood, and it can be divided into heritable, idiopathic drug- and toxin-induced and other disease (connective tissue disease, human immunodeficiency virus infection, portal hypertension, congenital heart disease, or schistosomiasis)-associated...
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Format: | Book |
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Elsevier,
2018-04-01T00:00:00Z.
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A1234.567 |
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