Deciphering the cause of Friedreich ataxia

This publication has 41 references indexed in Scilit:

• Evolution of the Friedreich’s ataxia trinucleotide repeat expansion: Founder effect and premutations
  Proceedings of the National Academy of Sciences, 1997
• Gene in the region of the Friedreich ataxia locus encodes a putative transmembrane protein expressed in the nervous system.
  Proceedings of the National Academy of Sciences, 1993
• Friedreich's ataxia: a descriptive epidemiological study in an Italian population
  Clinical Genetics, 1990
• Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia.
  Proceedings of the National Academy of Sciences, 1990
• “Acadian” and “classical” forms of Friedreich ataxia are most probably caused by mutations at the same locus
  American Journal of Medical Genetics, 1989
• Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker
  Genomics, 1989
• Mapping of mutation causing Friedreich's ataxia to human chromosome 9
  Nature, 1988
• Mitochondrial dysfunction and spinocerebellar degenerations
  Neurochemical Pathology, 1986
• FRIEDREICH'S ATAXIA: A CLINICAL AND GENETIC STUDY OF 90 FAMILIES WITH AN ANALYSIS OF EARLY DIAGNOSTIC CRITERIA AND INTRAFAMILIAL CLUSTERING OF CLINICAL FEATURES
  Brain, 1981
• Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's Ataxia
  Canadian Journal of Neurological Sciences, 1976