Transcriptomic profiling of unmethylated full mutation carriers implicates TET3 in FMR1 CGG repeat expansion methylation dynamics in fragile X syndrome.
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| Title: | Transcriptomic profiling of unmethylated full mutation carriers implicates TET3 in FMR1 CGG repeat expansion methylation dynamics in fragile X syndrome. |
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| Authors: | Farmiloe G; Evolutionary Neurogenomics, University of Amsterdam, Swammerdam Institute for Life Sciences, Science Park 904, Amsterdam, 1098XH, The Netherlands., Bejczy V; Evolutionary Neurogenomics, University of Amsterdam, Swammerdam Institute for Life Sciences, Science Park 904, Amsterdam, 1098XH, The Netherlands., Tabolacci E; Department of Life Sciences and Public Health, Section of Genomic Medicine, Catholic University, Rome, Italy.; Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy., Willemsen R; CBG-Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands., Jacobs F; Evolutionary Neurogenomics, University of Amsterdam, Swammerdam Institute for Life Sciences, Science Park 904, Amsterdam, 1098XH, The Netherlands. f.m.j.jacobs@uva.nl.; Amsterdam Neuroscience, Amsterdam, The Netherlands. f.m.j.jacobs@uva.nl. |
| Source: | Journal of neurodevelopmental disorders [J Neurodev Disord] 2025 Apr 26; Vol. 17 (1), pp. 22. Date of Electronic Publication: 2025 Apr 26. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101483832 Publication Model: Electronic Cited Medium: Internet ISSN: 1866-1955 (Electronic) Linking ISSN: 18661947 NLM ISO Abbreviation: J Neurodev Disord Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1866-1955 |
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| DOI: | 10.1186/s11689-025-09609-5 |
