GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co‐occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease

BACKGROUND: Congenital heart disease (CHD) is the most common birth defect and a major health problem around the world. However, its exact etiology has remained unclear. Among various genetic contributing factors, GATA4 transcription factor plays a significant role in the CHD pathogenesis. In this s...

Descripción completa

Detalles Bibliográficos
Autores principales: Kalayinia, Samira, Maleki, Majid, Rokni‐Zadeh, Hassan, Changi‐Ashtiani, Majid, Ahangar, Hassan, Biglari, Alireza, Shahani, Tina, Mahdieh, Nejat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757118/
https://www.ncbi.nlm.nih.gov/pubmed/31115957
http://dx.doi.org/10.1002/jcla.22923

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757118/
https://www.ncbi.nlm.nih.gov/pubmed/31115957
http://dx.doi.org/10.1002/jcla.22923

Ejemplares similares