Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome
Author:
Funder
Israel Science Foundation
Publisher
Frontiers Media SA
Subject
Cellular and Molecular Neuroscience,Molecular Biology
Reference55 articles.
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2. Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium;Bakker;Cell,1994
3. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation;Brouwer;Exp. Cell Res.,2007
4. CGG repeat-induced FMR1 silencing depends on the expansion size in human iPSCs and neurons carrying unmethylated full mutations;Brykczynska;Stem Cell Reports,2016
5. Prenatal diagnosis of fragile X syndrome: (CGG)n expansion and methylation of chorionic villus samples;Castellví-Bel;Prenat. Diagn.,1995
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