New cases of Glucose-6-Phosphate Dehydrogenase deficiency in Pulmonary Arterial Hypertension.

New cases of Glucose-6-Phosphate Dehydrogenase deficiency in Pulmonary Arterial Hypertension.

Pulmonary Arterial Hypertension (PAH) is a fatal disorder with limited treatment options and reduced life expectancy after diagnosis. Complex genetic backgrounds in PAH complicates identification of causative mutations that is essential for an understanding of the disease diagnostics and etiology es...

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Bibliographic Details
Main Authors: Sergey Kurdyukov, Cody A Eccles, Ankit A Desai, Manuel Gonzalez-Garay, Jason X-J Yuan, Joe G N Garcia, Olga Rafikova, Ruslan Rafikov
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0203493

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https://doi.org/10.1371/journal.pone.0203493

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