Defective Presynaptic Choline Transport Underlies Hereditary Motor Neuropathy

This publication has 27 references indexed in Scilit:

• The distal hereditary motor neuropathies
  Journal of Neurology, Neurosurgery & Psychiatry, 2011
• Lethal impairment of cholinergic neurotransmission in hemicholinium-3-sensitive choline transporter knockout mice
  Proceedings of the National Academy of Sciences, 2004
• Ultrastructural localization of high‐affinity choline transporter in the rat neuromuscular junction: Enrichment on synaptic vesicles
  Synapse, 2004
• The Choline Transporter Resurfaces: New Roles for Synaptic Vesicles?
  Molecular Interventions, 2004
• Vesicular Localization and Activity-Dependent Trafficking of Presynaptic Choline Transporters
  Journal of Neuroscience, 2003
• Aberrant Patterning of Neuromuscular Synapses in Choline Acetyltransferase-Deficient Mice
  Journal of Neuroscience, 2003
• Rapsyn Mutations in Humans Cause Endplate Acetylcholine-Receptor Deficiency and Myasthenic Syndrome
  The American Journal of Human Genetics, 2002
• Localization of the Gene for Distal Hereditary Motor Neuronopathy VII (dHMN-VII) to Chromosome 2q14
  The American Journal of Human Genetics, 2001
• Molecular Cloning of a Human, Hemicholinium-3-Sensitive Choline Transporter
  Biochemical and Biophysical Research Communications, 2000
• Mutation causing congenital myasthenia reveals acetylcholine receptor β/δ subunit interaction essential for assembly
  Journal of Clinical Investigation, 1999