Existence of mutations in the homeodomain-encoding region of NKX2.5 gene in Iranian patients with tetralogy of Fallot
Author:
Publisher
Medknow
Subject
General Medicine
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Case Report: Tetralogy of Fallot in a Chinese Family Caused by a Novel Missense Variant of MYOM2;Frontiers in Cardiovascular Medicine;2022-07-07
2. Accelerated Growth, Differentiation, and Ploidy with Reduced Proliferation of Right Ventricular Cardiomyocytes in Children with Congenital Heart Defect Tetralogy of Fallot;Cells;2022-01-05
3. A comprehensive overview of the medicinal chemistry of antifungal drugs: perspectives and promise;Chemical Society Reviews;2020
4. The Contribution of Gene Mutations to the Pathogenesisof Tetralogy of Fallot;International Journal of Basic Science in Medicine;2019-06-30
5. 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;Journal of Clinical Laboratory Analysis;2019-05-22
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