Limited phenotypic effects of selectively augmenting the SMN protein in the neurons of a mouse model of severe spinal muscular atrophy. [electronic resource]
Producer: 20130221Description: e46353 p. digitalISSN:- 1932-6203
- Animals
- Cellular Microenvironment
- Disease Models, Animal
- Female
- Genetic Therapy
- Humans
- Male
- Mice
- Mice, Transgenic
- Motor Activity
- Motor Neurons -- metabolism
- Muscular Atrophy, Spinal -- genetics
- Neuromuscular Junction -- genetics
- Organ Specificity
- Phenotype
- Severity of Illness Index
- Survival Rate
- Survival of Motor Neuron 1 Protein -- genetics
- Synapses -- genetics
- Transgenes
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
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