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Synaptic Defects in a Drosophila Model of Congenital Muscular Dystrophy
The congenital muscular dystrophies present in infancy with muscle weakness and are often associated with mental retardation. Many of these inherited disorders share a common etiology: defective O-glycosylation of α-dystroglycan, a component of the dystrophin complex. Protein-O-mannosyl transferase...
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| Publicado en: | J Neurosci |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Society for Neuroscience
2008
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6671091/ https://ncbi.nlm.nih.gov/pubmed/18385336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.0478-08.2008 |
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