Pathogenetic mechanisms of parkin in Parkinson's disease

This publication has 33 references indexed in Scilit:

• DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease
  Neurology, 2004
• Parkin disease: a phenotypic study of a large case series
  Brain, 2003
• Parkin mutations are frequent in patients with isolated early‐onset parkinsonism
  Brain, 2003
• Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial Parkinsonism associated with mutations in the Parkin gene
  Annals of Neurology, 2001
• Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
  Nature Genetics, 2000
• Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: Expanding the phenotype
  Annals of Neurology, 2000
• Association between Early-Onset Parkinson's Disease and Mutations in theParkinGene
  New England Journal of Medicine, 2000
• Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the Parkin gene in affected individuals
  Annals of Neurology, 1998
• Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q
  Neurology, 1998
• Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
  Nature, 1998