A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease

Introduction: Congenital heart disease (CHD) affects 1% to 2 % of live births. The Nkx2-5 gene, is known as the significant heart marker during embryonic evolution and it is also necessary for the survival of cardiomyocytes and homeostasis in adulthood. In this study, Nkx2-5 mutations are investigat...

Descripción completa

Detalles Bibliográficos
Autores principales: Kalayinia, Samira, Ghasemi, Serwa, Mahdieh, Nejat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891041/
https://www.ncbi.nlm.nih.gov/pubmed/31824610
http://dx.doi.org/10.15171/jcvtr.2019.47

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891041/
https://www.ncbi.nlm.nih.gov/pubmed/31824610
http://dx.doi.org/10.15171/jcvtr.2019.47

Ejemplares similares