The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds

Eitemau Tebyg

• The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus
  gan: Kwiatkowski, Thomas J., et al.
  Cyhoeddwyd: (1993)
• Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded.
  gan: Keats, B J, et al.
  Cyhoeddwyd: (1991)
• Molecular and Clinical Correlations in Spinocerebellar Ataxia Type I: Evidence for Familial Effects on the Age at Onset
  gan: Ranum, Laura P. W., et al.
  Cyhoeddwyd: (1994)
• Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I.
  gan: Jodice, C., et al.
  Cyhoeddwyd: (1994)
• Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.
  gan: Ranum, L P, et al.
  Cyhoeddwyd: (1991)