A Drosophila model of the neurological symptoms in Mpv17-related diseases

Mutations in the Mpv17 gene are responsible for MPV17-related hepatocerebral mitochondrial DNA depletion syndrome and Charcot–Marie–Tooth (CMT) disease. Although several models including mouse, zebrafish, and cultured human cells, have been developed, the models do not show any neurological defects,...

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Detalles Bibliográficos
Autores principales: Kodani, Atsushi, Yamaguchi, Mizuki, Itoh, Ririka, Huynh, Man Anh, Yoshida, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805426/
https://www.ncbi.nlm.nih.gov/pubmed/36587049
http://dx.doi.org/10.1038/s41598-022-27329-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805426/
https://www.ncbi.nlm.nih.gov/pubmed/36587049
http://dx.doi.org/10.1038/s41598-022-27329-x

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