Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome

European Journal of Human Genetics, Published online: 22 September 2023; doi:10.1038/s41431-023-01459-wMethylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown–Rahman syndrome

Source: European Journal of Human Genetics - September 22, 2023 Category: Genetics & Stem Cells Authors: Candy Kumps Erika D ’haenens Jennifer Kerkhof Haley McConkey Marielle Alders Bekim Sadikovic Olivier M. Vanakker Source Type: research