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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Detalhes bibliográficos
Publicado no:Front Med (Lausanne)
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Medicine
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8119639/
https://ncbi.nlm.nih.gov/pubmed/33996849
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fmed.2021.625763
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