Autosomal Dominant Cerebellar Ataxia Type III: Linkage in a Large British Family to a 7.6-cM Region on Chromosome 15q14-21.3

This publication has 27 references indexed in Scilit:

• Molecular and Clinical Study of 18 Families with ADCA Type II: Evidence for Genetic Heterogeneity and De Novo Mutation
  American Journal of Human Genetics, 1999
• Mapping of a New Autosomal Dominant Spinocerebellar Ataxia to Chromosome 22
  American Journal of Human Genetics, 1999
• Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel
  Nature Genetics, 1997
• Report of the Third International Workshop on Human Chromosome 15 Mapping 1996
  Cytogenetic and Genome Research, 1997
• Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
  Nature Genetics, 1996
• Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
  Nature Genetics, 1996
• Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
  Nature Genetics, 1996
• A comprehensive genetic map of the human genome based on 5,264 microsatellites
  Nature, 1996
• Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
  Nature Genetics, 1994
• THE CLINICAL FEATURES AND CLASSIFICATION OF THE LATE ONSET AUTOSOMAL DOMINANT CEREBELLAR ATAXIAS
  Brain, 1982