Hairpin Induced Slippage and Hyper-methylation of the Fragile X DNA Triplets
Author:
Publisher
Informa UK Limited
Subject
Molecular Biology,General Medicine,Structural Biology
Link
http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883
Reference30 articles.
1. An expanding story
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. Fragile X Genotype Characterized by an Unstable Region of DNA
4. Essential role for KH domains in RNA binding: Impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome
5. Triplet repeat mutations in human disease
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3. Epigenetic mechanism of FMR1 inactivation in Fragile X syndrome;The International Journal of Developmental Biology;2017
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