Human DNA Helicase B as a Candidate for Unwinding Secondary CGG Repeat Structures at the Fragile X Mental Retardation Gene
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DOI: 10.3389/fnmol.2018.00138
Abstract: The fragile X syndrome (FXS) is caused by a CGG repeat expansion at the fragile X mental retardation (FMR1) gene. FMR1 alleles with more than 200 CGG repeats bear chromosomal fragility when cells experience folate… read more here.
Keywords: dna; repeat; cgg; gene ... See more keywords