Correction: LRRK2 G2019S mutation contributes to mitochondrial transfer dysfunction in a Drp1-STX17-dependent manner

Key Points

• Mitochondrial transfer dysfunction has been linked to the LRRK2 G2019S mutation, suggesting critical pathways.
• Evidence shows that this mutation disrupts transfer functions through the Drp1-STX17 pathway.
• Assessment of cellular processes demonstrates how the G2019S mutation affects mitochondrial dynamics.
• These findings call for further exploration of targeted interventions in neurodegenerative diseases.