CGG repeats associated with fragile X chromosome form left-handed Z-DNA structure
Author:
Publisher
Wiley
Subject
Organic Chemistry,Biomaterials,Biochemistry,General Medicine,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/bip.21555/fullpdf
Reference44 articles.
1. Molecular-clinical correlations in males with an expanded FMR1 mutation
2. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
3. Methylation analysis of CGG sites in the CpG island of the human FMR1 gene
4. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
5. Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles
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4. Non-canonical DNA/RNA structures associated with the pathogenesis of Fragile X-associated tremor/ataxia syndrome and Fragile X syndrome;Frontiers in Genetics;2022-08-30
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