Inherited Neurodegenerative Disorders Caused by CAG/Polyglutamine Tract Expansions: Symposium Introduction
Author:
Publisher
Wiley
Subject
Neurology (clinical),Pathology and Forensic Medicine,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1750-3639.1997.tb00891.x/fullpdf
Reference10 articles.
1. Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
2. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
3. Trinucleotide repeat expansion in neurological disease
4. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
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