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AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats

BACKGROUND: Fragile X Syndrome (FXS), the most common inherited form of mental retardation, is caused by expansion of a CGG/CCG repeat tract in the 5′-untranslated region of the fragile X mental retardation (FMR1) gene, which changes the functional organization of the gene from euchromatin to hetero...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Volle, Catherine B, Delaney, Sarah
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2013
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3870987/
https://ncbi.nlm.nih.gov/pubmed/24261641
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2091-14-33
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