Glutamine repeats and neurodegenerative diseases: molecular aspects
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry
Reference40 articles.
1. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
2. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
3. Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansion
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5. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel
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