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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Detalles Bibliográficos
Autores principales: Kurdyukov, Sergey, Eccles, Cody A., Desai, Ankit A., Gonzalez-Garay, Manuel, Yuan, Jason X.-J., Garcia, Joe G. N., Rafikova, Olga, Rafikov, Ruslan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117081/
https://www.ncbi.nlm.nih.gov/pubmed/30161219
http://dx.doi.org/10.1371/journal.pone.0203493

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6117081/
https://www.ncbi.nlm.nih.gov/pubmed/30161219
http://dx.doi.org/10.1371/journal.pone.0203493

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