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Abnormal mitochondrial transport and morphology as early pathological changes in human models of spinal muscular atrophy
Spinal muscular atrophy (SMA), characterized by specific degeneration of spinal motor neurons, is caused by mutations in the survival of motor neuron 1, telomeric (SMN1) gene and subsequent decreased levels of functional SMN. How the deficiency of SMN, a ubiquitously expressed protein, leads to spin...
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| Publicado no: | Dis Model Mech |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Ltd
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4728333/ https://ncbi.nlm.nih.gov/pubmed/26586529 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.021766 |
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