Close Associations between Prevalences of Dominantly Inherited Spinocerebellar Ataxias with CAG-Repeat Expansions and Frequencies of Large Normal CAG Alleles in Japanese and Caucasian Populations

This publication has 38 references indexed in Scilit:

• Contribution of DNA Sequence and CAG Size to Mutation Frequencies of Intermediate Alleles for Huntington Disease: Evidence from Single Sperm Analyses
  Human Molecular Genetics, 1997
• Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel
  Nature Genetics, 1997
• Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum
  Human Molecular Genetics, 1995
• Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease
  Human Molecular Genetics, 1995
• Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patients
  Human Molecular Genetics, 1995
• Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23–q24.1
  Genomics, 1995
• DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence
  Human Molecular Genetics, 1994
• Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene
  Nature Genetics, 1994
• Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence
  Nature Genetics, 1994
• De novo expansion of a (CAG)n repeat in sporadic Huntington's disease
  Nature Genetics, 1993