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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Publié dans:J Neurosci
Auteurs principaux: Wairkar, Yogesh P., Fradkin, Lee G., Noordermeer, Jasprina N., DiAntonio, Aaron
Format: Artigo
Langue:Inglês
Publié: Society for Neuroscience 2008
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Articles
Accès en ligne: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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