Associated Papers
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease.
Tabrizi F et al.
Molecular Biology Reports, 2024
HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.
Wang J et al.
Pediatric Cardiology, 2017
Chromosome 5q33 deletions associated with congenital heart defects.
Starkovich M et al.
American Journal of Medical Genetics. Part A, 2016
Investigation of somatic NKX2-5, GATA4 and HAND1 mutations in patients with tetralogy of Fallot.
Wang J et al.
Pathology, 2011
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