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Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors
Angelman syndrome (AS) is a childhood-onset neurogenetic disorder characterized by functionally severe developmental delay with mental retardation, deficits in expressive language, ataxia, appendicular action tremors and unique behaviors such as inappropriate laughter and stimulus-sensitive hyperexc...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2008
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2902285/ https://ncbi.nlm.nih.gov/pubmed/18413322 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn117 |
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