Human Ku Antigen Tightly Binds and Stabilizes a Tetrahelical Form of the Fragile X Syndrome d(CGG) Expanded Sequence
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference59 articles.
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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 Sites on Human Chromosomes: Demonstration of Their Dependence on the Type of Tissue Culture Medium
4. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
5. Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n
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