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Loss of RAB39B does not alter MPTP-induced Parkinson’s disease-like phenotypes in mice
Parkinson’s disease (PD) is a common neurodegenerative movement disorder with undetermined etiology. A major pathological hallmark of PD is the progressive degeneration of dopaminergic neurons in the substantia nigra. Loss-of-function mutations in the RAB39B gene, which encodes a neuronal-specific s...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9905435/ https://www.ncbi.nlm.nih.gov/pubmed/36761179 http://dx.doi.org/10.3389/fnagi.2023.1087823 |