[HTML][HTML] Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown–Rahman syndrome
D Zebrauskiene, E Sadauskiene, J Dapkunas… - Clinical …, 2024 - ncbi.nlm.nih.gov
Abstract Tatton-Brown–Rahman syndrome (TBRS) is a rare congenital genetic disorder
caused by autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A …
caused by autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A …
[HTML][HTML] Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown–Rahman syndrome
D Zebrauskiene, E Sadauskiene… - Clinical …, 2024 - clinicalepigeneticsjournal …
Tatton-Brown–Rahman syndrome (TBRS) is a rare congenital genetic disorder caused by
autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A gene …
autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A gene …
Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown-Rahman syndrome
D Zebrauskiene, E Sadauskiene… - Clinical …, 2024 - pubmed.ncbi.nlm.nih.gov
Tatton-Brown-Rahman syndrome (TBRS) is a rare congenital genetic disorder caused by
autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A gene …
autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A gene …
Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown-Rahman syndrome.
D Zebrauskiene, E Sadauskiene, J Dapkunas… - Clinical …, 2024 - europepmc.org
Tatton-Brown-Rahman syndrome (TBRS) is a rare congenital genetic disorder caused by
autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A gene …
autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A gene …
Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown–Rahman syndrome.
D Zebrauskiene, E Sadauskiene… - Clinical …, 2024 - search.ebscohost.com
Abstract Tatton-Brown–Rahman syndrome (TBRS) is a rare congenital genetic disorder
caused by autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A …
caused by autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A …
[PDF][PDF] Aortic disease and cardiomyopathy in patients with a novel DNMT3A gene variant causing Tatton-Brown–Rahman syndrome
D Zebrauskiene, E Sadauskiene, J Dapkunas… - 2024 - clinicalepigeneticsjournal …
Abstract Tatton-Brown–Rahman syndrome (TBRS) is a rare congenital genetic disorder
caused by autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A …
caused by autosomal dominant pathogenic variants in the DNA methyltransferase DNMT3A …