Novel TNIP2 and TRAF2 Variants Are Implicated in the Pathogenesis of Pulmonary Arterial Hypertension

Background: Pulmonary arterial hypertension (PAH) is a rare disease characterized by pulmonary vascular remodeling and right heart failure. Specific genetic variants increase the incidence of PAH in carriers with a family history of PAH, those who suffer from certain medical conditions, and even tho...

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Detalles Bibliográficos
Autores principales: Pienkos, Shaun, Gallego, Natalia, Condon, David F., Cruz-Utrilla, Alejandro, Ochoa, Nuria, Nevado, Julián, Arias, Pedro, Agarwal, Stuti, Patel, Hiral, Chakraborty, Ananya, Lapunzina, Pablo, Escribano, Pilar, Tenorio-Castaño, Jair, de Jesús Pérez, Vinicio A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119639/
https://www.ncbi.nlm.nih.gov/pubmed/33996849
http://dx.doi.org/10.3389/fmed.2021.625763

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119639/
https://www.ncbi.nlm.nih.gov/pubmed/33996849
http://dx.doi.org/10.3389/fmed.2021.625763

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