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Abnormally increased surface expression of AMPA receptors in the cerebellum, cortex and striatum of Cln3(−/−) mice
Mutations in the CLN3 gene cause a fatal neurodegenerative disorder, juvenile CLN3 disease. Exploring the cause of the motor coordination deficit in the Cln3(−/−) mouse model of the disease we have previously found that attenuation of AMPA receptor activity in 1-month-old Cln3(−/−) mice significantl...
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| Publicat a: | Neurosci Lett |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4631631/ https://ncbi.nlm.nih.gov/pubmed/26375929 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2015.09.012 |
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