Altered hippocampal gene expression, glial cell population, and neuronal excitability in aminopeptidase P1 deficiency
Abstract Inborn errors of metabolism are often associated with neurodevelopmental disorders and brain injury. A deficiency of aminopeptidase P1, a proline-specific endopeptidase encoded by the Xpnpep1 gene, causes neurological complications in both humans and mice. In addition, aminopeptidase P1-def...
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Format: | article |
Langue: | EN |
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Nature Portfolio
2021
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Accès en ligne: | https://doaj.org/article/97a9a9fc35484ae295a4e9f21a1be55a |
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