Mitochondrial impairment and synaptic dysfunction are associated with neurological defects in iPSCs-derived cortical neurons of MERRF patients
Abstract Background Myoclonic epilepsy with ragged-red fibers (MERRF) syndrome is a rare inherited mitochondrial disease mainly caused by the m.8344A > G mutation in mitochondrial tRNALys gene, and usually manifested as complex neurological disorders and muscle weakness. Currently, the pathogenic...
Auteurs principaux: | , , , , , |
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Format: | Article |
Langue: | English |
Publié: |
BMC
2023-08-01
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Collection: | Journal of Biomedical Science |
Sujets: | |
Accès en ligne: | https://doi.org/10.1186/s12929-023-00966-8 |