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...

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Publicado en:Eurasian J Med
Autores principales: El Bouchikhi, Ihssane, Bouguenouch, Laila, Moufid, Fatima Zohra, Belhassan, Khadija, Samri, Imane, Chaouti, Amal, Houssaïni, Mohammed Iraqui, Atmani, Samir, Ouldim, Karim
Formato: Artigo
Lenguaje:Inglês
Publicado: The Eurasian Journal of Medicine 2020
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Original Article
Acceso en línea: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
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