Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy.

Proximal spinal muscular atrophy (SMA) is a common autosomal recessive childhood form of motor neuron disease. Previous studies have highlighted nerve- and muscle-specific events in SMA, including atrophy of muscle fibres and post-synaptic motor endplates, loss of lower motor neuron cell bodies and...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awduron: Murray, L, Comley, L, Thomson, D, Parkinson, N, Talbot, K, Gillingwater, T
Fformat: Journal article
Iaith:English
Cyhoeddwyd: 2008