An EGLN1 mutation may regulate hypoxic response in cyanotic congenital heart disease through the PHD2/HIF-1A pathway

Cyanotic congenital heart disease (CCHD), a term describing the most severe congenital heart diseases are characterized by the anatomic malformation of a right to left shunt. Although the incidence of CCHD are far less than the that of congenital heart diseases (CHD), patients with CCHD always prese...

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Detalles Bibliográficos
Autores principales: Zhou, Yuanlin, Ouyang, Na, Liu, Lingjuan, Tian, Jie, Huang, Xupei, Lu, Tiewei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411777/
https://www.ncbi.nlm.nih.gov/pubmed/30906831
http://dx.doi.org/10.1016/j.gendis.2018.03.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411777/
https://www.ncbi.nlm.nih.gov/pubmed/30906831
http://dx.doi.org/10.1016/j.gendis.2018.03.003

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