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SMN is required for sensory-motor circuit function in Drosophila
Spinal muscular atrophy (SMA) is a lethal human disease characterized by motor neuron dysfunction and muscle deterioration due to depletion of the ubiquitous Survival Motor Neuron (SMN) protein. Drosophila SMN mutants have reduced muscle size and defective locomotion, motor rhythm and motor neuron n...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3475188/ https://ncbi.nlm.nih.gov/pubmed/23063130 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2012.09.011 |
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