Huntington's disease gene (IT15) is widely expressed in human and rat tissues

This publication has 33 references indexed in Scilit:

• Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
  Nature, 1993
• Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome
  Nature Genetics, 1993
• A point mutation in the FMR-1 gene associated with fragile X mental retardation
  Nature Genetics, 1993
• Heritable unstable DNA sequences
  Nature Genetics, 1992
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Absence of expression of the FMR-1 gene in fragile X syndrome
  Cell, 1991
• Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
  Published by Elsevier ,1991
• The functional anatomy of basal ganglia disorders
  Trends in Neurosciences, 1989
• Huntingtons Disease
  New England Journal of Medicine, 1986
• Motor neuron diseases and amyotrophic lateral sclerosis
  Trends in Neurosciences, 1984