Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot
Author:
Publisher
Elsevier BV
Subject
Pathology and Forensic Medicine
Reference29 articles.
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1. Molecular and cellular role of variants of the promoter region of HAND1 gene in sporadic and isolated ventricular septal defect;Molecular and Cellular Biochemistry;2024-08-06
2. NKX2.5 coding exons sequencing reveals novel non-synonymous mutations in patients with sporadic congenital heart diseases among the Tanzanian population;Egyptian Journal of Medical Human Genetics;2024-07-31
3. Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease;Molecular Biology Reports;2024-03-29
4. Sequence variations in GATA4 and CITED2 gene among patients with cardiac septation defects from Xinjiang, China;Cardiology in the Young;2024-03-08
5. Somatic GATA4 mutation contributes to tetralogy of Fallot;Experimental and Therapeutic Medicine;2024-01-08
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