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- W2049156476 endingPage "76" @default.
- W2049156476 startingPage "65" @default.
- W2049156476 abstract "Fragile X mental retardation syndrome, FRAXE mental retardation, Progressive myoclonus epilepsy Type I, and Friedreich ataxia are members of a larger group of genetic disorders known as the Repeat Expansion Diseases. Unlike other members of this group, these four disorders all result from a primary defect in the initiation or elongation of transcription. In this review, we discuss current models for the relationship between the expanded repeat and the disease symptoms." @default.
- W2049156476 created "2016-06-24" @default.
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- W2049156476 date "2003-01-01" @default.
- W2049156476 modified "2023-10-14" @default.
- W2049156476 title "Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia" @default.
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- W2049156476 doi "https://doi.org/10.1159/000072839" @default.
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