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ALLN rescues an in vitro excitatory synaptic transmission deficit in Lis1 mutant mice
LIS1 gene mutations lead to a rare neurological disorder, classical lissencephaly, characterized by brain malformations, mental retardation, seizures, and premature death. Mice heterozygous for Lis1 (Lis1(+/−)) exhibit cortical malformations, defects in neuronal migration, increased glutamate-mediat...
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| Auteurs principaux: | , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Physiological Society
2013
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3545457/ https://ncbi.nlm.nih.gov/pubmed/23100132 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/jn.00431.2012 |
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