A spinal muscular atrophy modifier implicates the SMN protein in SNARE complex assembly at neuromuscular synapses

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• The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn-/- mice and results in a mouse with spinal muscular atrophy
  gan: Umrao R. Monani
  Cyhoeddwyd: (2000)
• Reduced Survival of Motor Neuron (SMN) Protein in Motor Neuronal Progenitors Functions Cell Autonomously to Cause Spinal Muscular Atrophy in Model Mice Expressing the Human Centromeric (SMN2) Gene
  gan: Park, Gyu-Hwan, et al.
  Cyhoeddwyd: (2010)
• Muscle-specific SMN reduction reveals motor neuron–independent disease in spinal muscular atrophy models
  gan: Jeong-Ki Kim, et al.
  Cyhoeddwyd: (2020)
• Emerging concepts underlying selective neuromuscular dysfunction in infantile-onset spinal muscular atrophy
  gan: Gollapalli, Kishore, et al.
  Cyhoeddwyd: (2021)
• Reduced Survival of Motor Neuron (SMN) Protein in Motor Neuronal Progenitors Functions Cell Autonomously to Cause Spinal Muscular Atrophy in Model Mice Expressing the Human Centromeric (<i>SMN2</i>) Gene
  gan: Gyu-Hwan Park, et al.
  Cyhoeddwyd: (2010)