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

**Authors:** Mei Ding, Fen Wang, Lan‑Lan Jiang, Chao Ma, Yu‑Wan Qi, Jun‑Yi Liu, Juan Li, Mei‑Xia Wang, Hong Jin, Jin‑Ru Zhang, Cheng‑Jie Mao, Xiao‑Kang Li, Chun‑Feng Liu, Xiao‑Yu Cheng

PMC · DOI: 10.1186/s40035-025-00533-1 · 2026-02-14

## Full-text entities

- **Genes:** STX17 (syntaxin 17) [NCBI Gene 55014], UTRN (utrophin) [NCBI Gene 7402] {aka DMDL, DRP, DRP1}, LRRK2 (leucine rich repeat kinase 2) [NCBI Gene 120892] {aka AURA17, DARDARIN, PARK8, RIPK7, ROCO2}
- **Diseases:** mitochondrial transfer dysfunction (MESH:D028361)
- **Mutations:** G2019S

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12905968/full.md

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Source: https://tomesphere.com/paper/PMC12905968