Neuropathology does not Correlate with Regional Differences in the Extent of Expansion of CTG Repeats in the Brain with Myotonic Dystrophy Type 1
Author:
Affiliation:
1. Department of Pathology and Applied Neurobiology, Kyoto Prefectural University of Medicine, Graduate School of Medical Science
2. Department of Neurology, National Hospital Organization Hyogo-Chuo National Hospital
Publisher
Japan Society of Histochemistry & Cytochemistry
Subject
Cell Biology,Histology,Physiology,Biochemistry,Pathology and Forensic Medicine
Link
http://www.jstage.jst.go.jp/article/ahc/43/6/43_10019/_pdf
Reference34 articles.
1. Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon
2. 2. Ashizawa, T. (1998) Myotonic dystrophy as a brain disorder. Arch. Neurol. 55; 291-293.
3. Cloning of the essential myotonic dystrophy region and mapping of the putative defect
4. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
5. Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts
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