Association of NFKB1, NKX2-5, GATA4 and RANKL Gene Polymorphisms with Sporadic Congenital Heart Disease in Greek Patients

Congenital heart disease (CHD) is a group of structural defects of the heart and the great vessels, and one of the leading causes of death among infants and young adults. Several gene variants are involved in diverse mechanisms of cardiac and vessel development and could thus be considered candidate...

Descripción completa

Detalles Bibliográficos
Autores principales: Aidinidou, L, Chatzikyriakidou, A, Giannopoulos, A, Karpa, V, Tzimou, I, Aidinidou, E, Fidani, L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366470/
https://www.ncbi.nlm.nih.gov/pubmed/34447654
http://dx.doi.org/10.2478/bjmg-2021-0014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366470/
https://www.ncbi.nlm.nih.gov/pubmed/34447654
http://dx.doi.org/10.2478/bjmg-2021-0014

Ejemplares similares