Mapping of Spinocerebellar Ataxia 13 to Chromosome 19q13.3-q13.4 in a Family with Autosomal Dominant Cerebellar Ataxia and Mental Retardation

This publication has 25 references indexed in Scilit:

• Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology
  European Journal of Human Genetics, 2000
• Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12
  Nature Genetics, 1999
• Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias
  Human Molecular Genetics, 1996
• A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands
  Human Molecular Genetics, 1996
• A comprehensive genetic map of the human genome based on 5,264 microsatellites
  Nature, 1996
• Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias
  Nature, 1995
• Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations
  Annals of Neurology, 1995
• A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus.
  1994
• Faster sequential genetic linkage computations.
  1993
• Clinical features and classification of inherited ataxias.
  1993