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The Dystrophin Dp186 Isoform Regulates Neurotransmitter Release at a Central Synapse in Drosophila

The Dystrophin protein is encoded by a gene that, when mutated in humans, can cause Duchenne muscular dystrophy, a disease characterized by progressive muscle wasting. A number of Duchenne patients also exhibit poorly understood mental retardation, likely associated with loss of a brain-specific iso...

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Detalhes bibliográficos
Main Authors: Fradkin, Lee G., Baines, Richard A., van der Plas, Mariska C., Noordermeer, Jasprina N.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2408742/
https://ncbi.nlm.nih.gov/pubmed/18463264
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4950-07.2008
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