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Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures

Fragile X syndrome is caused by expansion of a d(CGG) trinucleotide repeat sequence in the 5′ untranslated region of the first exon of the FMR1 gene. Repeat expansion is thought to be instigated by formation of d(CGG)(n) secondary structures. Stable FMR1 d(CGG)(n) runs in normal individuals consist...

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Udgivet i:Nucleic Acids Res
Principais autores: Weisman-Shomer, Pnina, Cohen, Esther, Fry, Michael
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2000
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Article
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC102797/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10710419/
https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/28.7.1535
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