Description of Two New Cases of AQP1 Related Pulmonary Arterial Hypertension and Review of the Literature

Pulmonary arterial hypertension (PAH) is a severe clinical condition characterized by an increase in mean pulmonary artery pressure, which leads to a right ventricular hypertrophy and potentially heart failure and death. In the last several years, many genes have been associated with PAH, particular...

Descripción completa

Detalles Bibliográficos
Autores principales: Gallego-Zazo, Natalia, Cruz-Utrilla, Alejandro, del Cerro, María Jesús, Ochoa Parra, Nuria, Blanco, Julián Nevado, Arias, Pedro, Lapunzina, Pablo, Escribano-Subias, Pilar, Tenorio-Castaño, Jair
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141352/
https://www.ncbi.nlm.nih.gov/pubmed/35627312
http://dx.doi.org/10.3390/genes13050927

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141352/
https://www.ncbi.nlm.nih.gov/pubmed/35627312
http://dx.doi.org/10.3390/genes13050927

Ejemplares similares