Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects

OBJECTIVE: Atrial septal defect (ASD) is one of the most common types of congenital heart disease (CHD). It is mainly caused by mutations of NK2 homeobox 5, GATA binding protein 4 (GATA4), and myosin heavy chain 6 in non-syndromic cases. This study aims to carry out, for the first time, the GATA4 mu...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Eurasian J Med
Main Authors: El Bouchikhi, Ihssane, Bouguenouch, Laila, Moufid, Fatima Zohra, Belhassan, Khadija, Samri, Imane, Chaouti, Amal, Houssaïni, Mohammed Iraqui, Atmani, Samir, Ouldim, Karim
Formato: Artigo
Idioma:Inglês
Publicado em: The Eurasian Journal of Medicine 2020
Assuntos:
Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7651766/
https://ncbi.nlm.nih.gov/pubmed/33209082
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/eurasianjmed.2020.19237
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados