Histone Modifications Depict an Aberrantly Heterochromatinized FMR1 Gene in Fragile X Syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference37 articles.
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3. Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes;Boggs;Nat Genet,2002
4. The structure of mouse HP1 suggests a unique mode of single peptide recognition by the shadow chromodomain dimer;Brasher;EMBO J,2000
5. Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene;Chiurazzi;Hum Mol Genet,1999
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