Literature DB >> 14526165

Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia.

E Greene1, V Handa, D Kumari, K Usdin.   

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. Copyright 2003 S. Karger AG, Basel

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Year:  2003        PMID: 14526165     DOI: 10.1159/000072839

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  1 in total

1.  Trend-TDT - a transmission/disequilibrium based association test on functional mini/microsatellites.

Authors:  Bing-Jian Feng; David E Goldgar; Marilys Corbex
Journal:  BMC Genet       Date:  2007-11-01       Impact factor: 2.797

  1 in total

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