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Stability of the Human Fragile X (CGG)(n) Triplet Repeat Array in Saccharomyces cerevisiae Deficient in Aspects of DNA Metabolism

Expanded trinucleotide repeats underlie a growing number of human diseases. The human FMR1 (CGG)(n) array can exhibit genetic instability characterized by progressive expansion over several generations leading to gene silencing and the development of the fragile X syndrome. While expansion is depend...

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Publicat a:Mol Cell Biol
Autors principals: White, Peter J., Borts, Rhona H., Hirst, Mark C.
Format: Artigo
Idioma:Inglês
Publicat: Taylor & Francis 1999
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Accés en línia:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC84419/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10409756/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/mcb.19.8.5675
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