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Homeostasis of the astrocytic glutamate transporter GLT-1 is altered in mouse models of Lafora disease
Lafora disease (LD, OMIM 254780) is a fatal rare disorder characterized by epilepsy and neurodegeneration. Although in recent years a lot of information has been gained on the molecular basis of the neurodegeneration that accompanies LD, the molecular basis of epilepsy is poorly understood. Here, we...
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| Pubblicato in: | Biochim Biophys Acta |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5472677/ https://ncbi.nlm.nih.gov/pubmed/26976331 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbadis.2016.03.008 |
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