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Altered glutamate receptor function in the cerebellum of the Ppt1(−/−) mouse, a murine model of infantile neuronal ceroid lipofuscinosis
The neuronal ceroid lipofuscinoses (NCLs) are a family of devastating pediatric neurodegenerative disorders and currently represent the most common form of pediatric-onset neurodegeneration. Infantile NCL (INCL), the most aggressive of these disorders, is caused by mutations in the CLN1 gene that en...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3237775/ https://ncbi.nlm.nih.gov/pubmed/21971706 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jnr.22763 |
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