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Persistent motor dysfunction despite homeostatic rescue of cerebellar morphogenesis in the Car8 waddles mutant mouse
BACKGROUND: Purkinje cells play a central role in establishing the cerebellar circuit. Accordingly, disrupting Purkinje cell development impairs cerebellar morphogenesis and motor function. In the Car8(wdl) mouse model of hereditary ataxia, severe motor deficits arise despite the cerebellum overcomi...
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| Gepubliceerd in: | Neural Dev |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2019
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6417138/ https://ncbi.nlm.nih.gov/pubmed/30867000 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13064-019-0130-4 |
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