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Central biogenic amine deficiency with concomitant exploratory behavioral deficits in Dnajc12 knock-out mice

Abstract Bi-allelic autosomal recessive pathogenic variants in DNAJC12 lead to a constellation of neurological features, including young-onset Parkinson’s disease. DNAJC12 is a co-chaperone for enzymes involved in biogenic amines synthesis. In vitro, we discovered overexpressed DNAJC12 forms a compl...

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Bibliografische gegevens
Hoofdauteurs: Isaac Bul Deng, Jordan Follett, Jesse D. Fox, Shannon Wall, Matthew J. Farrer
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Nature Portfolio 2025-05-01
Reeks:npj Parkinson's Disease
Online toegang:https://doi.org/10.1038/s41531-025-00991-4
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