Deconstructing myotonic dystrophy
- PMID: 11001736
- DOI: 10.1126/science.289.5485.1701
Deconstructing myotonic dystrophy
Abstract
Triplet repeat diseases are disorders in which there is expansion of a repeat sequence of three nucleotides in the affected gene. Although the pathology usually results from production of a defective protein, myotonic dystrophy (DM) has proved to be a puzzle because the expanded repeats appear in a non-coding region of the affected DMPK gene. In a Perspective, Tapscott explains how findings from a new mouse model of DM (Mankodi et al.) could solve this paradox.
Comment on
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Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat.Science. 2000 Sep 8;289(5485):1769-73. doi: 10.1126/science.289.5485.1769. Science. 2000. PMID: 10976074
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