NKX2-5 Gene Variants Associated with Congenital Heart Defects in Turkish Population

NKX2-5 Gene Variants Associated with Congenital Heart Defects in Turkish Population

Introduction: Congenital heart defects (CHDs) are the most common congenital anomaly of the newborn with high mortality and morbidity rates. Genetic and environmental risk factors have affect on cardiogenesis. NKX2-5 (NK2 homeobox 5) is a homeobox containing gene which is essential for cardiac diffe...

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Bibliographic Details
Main Authors: Bilgen Bilge Geçkinli, Gözde Girgin Özgümüş, Şenol Demir, Ayberk Türkyilmaz, Figen Akalın
Format: Article
Language:English
Published: Galenos Publishing House 2024-12-01
Series:Güncel Pediatri
Subjects:
congenital heart defects
nkx2-5 gene
tetralogy of fallot
patent foramen ovale
atrial septal defect
Online Access:https://www.guncelpediatri.com/articles/nkx2-5-gene-variants-associated-with-congenital-heart-defects-in-turkish-population/doi/jcp.2024.69376
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https://www.guncelpediatri.com/articles/nkx2-5-gene-variants-associated-with-congenital-heart-defects-in-turkish-population/doi/jcp.2024.69376

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