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Updated: May 15, 2026

Dissection of the Transversus Abdominis Muscle for Whole-mount Neuromuscular Junction Analysis
Published on: January 11, 2014
Spinal muscular atrophy, John Griffin, and mentorship
1Department of Neurology; Department of Neuroscience, Johns Hopkins School of Medicine, 855 North Wolfe St., Baltimore, MD 21205, USA. csumner1@jhmi.edu
Abstract:
Hereditary canine spinal muscular atrophy is an inherited motor neuron disease that occurs in Brittany Spaniels and has remarkable similarities with human spinal muscular atrophy. Both disorders are characterized by proximal limb and truncal muscle weakness of variable severity. Detailed pathological studies indicate that there is early dysfunction of motor neuron synapses, particularly the neuromuscular junction synapse, prior to motor neuron death. This period of synaptic dysfunction may define a critical window of opportunity for disease reversibility in motor neuron disease.
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