Molecular genetics and pathogenesis of Friedreich ataxia

This publication has 35 references indexed in Scilit:

• Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes
  Human Molecular Genetics, 1997
• Evolution of the Friedreich’s ataxia trinucleotide repeat expansion: Founder effect and premutations
  Proceedings of the National Academy of Sciences, 1997
• Regulation of Mitochondrial Iron Accumulation by Yfh1p, a Putative Homolog of Frataxin
  Science, 1997
• Frataxin fracas
  Nature Genetics, 1997
• The Friedreich's ataxia gene encodes a novel phosphatidylinositol–4–phosphate 5–kinase
  Nature Genetics, 1996
• Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion
  Science, 1996
• Friedreich's ataxia: a defect in signal transduction?
  Human Molecular Genetics, 1995
• Mapping of mutation causing Friedreich's ataxia to human chromosome 9
  Nature, 1988
• Recessive ataxia in Acadians and “Cajuns”
  Canadian Journal of Neurological Sciences, 1984
• A Cluster of Friedreich's Ataxia in Rimouski, Québec
  Canadian Journal of Neurological Sciences, 1979