Correction: LRRK2 G2019S mutation contributes to mitochondrial transfer dysfunction in a Drp1-STX17-dependent manner
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
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsMitochondrial Function and Pathology · Genetic Neurodegenerative Diseases · Metabolism and Genetic Disorders