Associated Papers
Identification of deleterious single nucleotide polymorphism (SNP)s in the human TBX5 gene & prediction of their structural & functional consequences: An in silico approach.
Mahfuz AMUB et al.
Biochemistry and Biophysics Reports, 2021
Functional analysis of two novel TBX5 variants present in individuals with Holt-Oram syndrome with different clinical manifestations.
Varela D et al.
Molecular Genetics and Genomics : Mgg, 2021
Familial dilated cardiomyopathy associated with pathogenic TBX5 variants: Expanding the cardiac phenotype associated with Holt-Oram syndrome.
Patterson J et al.
American Journal of Medical Genetics. Part A, 2020
Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age: A next-generation sequencing study.
Hata Y et al.
Heart Rhythm, 2016
Intermolecular Interactions of Cardiac Transcription Factors NKX2.5 and TBX5.
Pradhan L et al.
Biochemistry, 2016
A novel TBX5 loss-of-function mutation associated with sporadic dilated cardiomyopathy.
Zhou W et al.
International Journal of Molecular Medicine, 2015
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