Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome
Author:
Funder
Fondazione Telethon
Publisher
MDPI AG
Subject
Genetics(clinical),Genetics
Link
http://www.mdpi.com/2073-4425/7/8/49/pdf
Reference77 articles.
1. FMR1 and the fragile X syndrome: Human genome epidemiology review
2. Autism Spectrum Phenotype in Males and Females with Fragile X Full Mutation and Premutation
3. Evidence for Altered Fragile-X Mental Retardation Protein Expression in Response to Behavioral Stimulation
4. Epidemiology of fragile X syndrome: A systematic review and meta-analysis
5. A marker X chromosome;Lubs;Am. J. Hum. Genet.,1969
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2. Variation of FMRP Expression in Peripheral Blood Mononuclear Cells from Individuals with Fragile X Syndrome;Genes;2024-03-13
3. Epigenetic causes of intellectual disability—the fragile X syndrome paradigm;Neuropsychiatric Disorders and Epigenetics;2024
4. Antisense oligonucleotide rescue of CGG expansion–dependent FMR1 mis-splicing in fragile X syndrome restores FMRP;Proceedings of the National Academy of Sciences;2023-06-26
5. The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study;Journal of Neurodevelopmental Disorders;2022-12
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