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  • Richard R Ribchester, Derek S. Thomson, +5 authors A. Jennifer Morton
  • Biology, Medicine
  • The European journal of neuroscience
  • 2004 (First Publication: 2 December 2004)
  • Huntington's disease (HD) is a neurodegenerative disorder with complex symptoms dominated by progressive motor dysfunction. Skeletal muscle atrophy is common in HD patients. Because the HD mutationExpand
  • Thomas M. Wishart, Timothy M. Rooney, +5 authors Thomas H. Gillingwater
  • Medicine, Biology
  • PLoS genetics
  • 2012 (First Publication: 1 August 2012)
  • Degeneration of synaptic and axonal compartments of neurons is an early event contributing to the pathogenesis of many neurodegenerative diseases, but the underlying molecular mechanisms remainExpand
  • Sarah M. Carpanini, Lisa Mckie, +11 authors Ian J. Jackson
  • Biology, Medicine
  • Disease Models & Mechanisms
  • 2014 (First Publication: 24 April 2014)
  • Mutations in RAB18 have been shown to cause the heterogeneous autosomal recessive disorder Warburg Micro syndrome (WARBM). Individuals with WARBM present with a range of clinical symptoms, includingExpand