Deficiency of Mitochondrial Aspartate-Glutamate Carrier 1 Leads to Oligodendrocyte Precursor Cell Proliferation Defects Both In Vitro and In Vivo

Aspartate-Glutamate Carrier 1 (AGC1) deficiency is a rare neurological disease caused by mutations in the solute carrier family 25, member 12 (SLC25A12) gene, encoding for the mitochondrial aspartate-glutamate carrier isoform 1 (AGC1), a component of the malate–aspartate NADH shuttle (MAS), expresse...

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Detalhes bibliográficos
Publicado no:Int J Mol Sci
Main Authors: Petralla, Sabrina, Peña-Altamira, Luis Emiliano, Poeta, Eleonora, Massenzio, Francesca, Virgili, Marco, Barile, Simona Nicole, Sbano, Luigi, Profilo, Emanuela, Corricelli, Mariangela, Danese, Alberto, Giorgi, Carlotta, Ostan, Rita, Capri, Miriam, Pinton, Paolo, Palmieri, Ferdinando, Lasorsa, Francesco Massimo, Monti, Barbara
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6769484/
https://ncbi.nlm.nih.gov/pubmed/31514314
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms20184486
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