Transcriptomic profiling of unmethylated full mutation carriers implicates TET3 in FMR1 CGG repeat expansion methylation dynamics in Fragile X syndrome
Grace Farmiloe, Veronika Bejczy, Elisabetta Tabolacci, Rob Willemsen, Frank M. J. Jacobs
The paper identifies TET3 downregulation in unmethylated FMR1 full mutation carriers and suggests it may contribute to the lack of methylation in FXS.
Journal of Neurodevelopmental Disorders · Apr 26, 2025Peer-reviewedNeuroscience