Publications by authors named "Shunyan Hong"

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A Homoplasmic MT-TV Mutation Associated with Mitochondrial Inheritance of Hereditary Spastic Paraplegia.
Yan Shi, Junhao Xie, Junyi Jiang, Xinyu Yan, Xuejiao Chen, Shunyan Hong

Mov Disord· January 2025

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Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization.
Xiang Lin, Jun-Yi Jiang, Dao-Jun Hong, Kai-Jun Lin, Jin-Jing Li, Shunyan Hong

Mov Disord· January 2024

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Loss of function of CMPK2 causes mitochondria deficiency and brain calcification.
Miao Zhao, Hui-Zhen Su, Yi-Heng Zeng, Yuan Sun, Xin-Xin Guo, Chong Wang, Shunyan Hong, Hong-Tao Wang, Xiao-Hong Lin

Cell Discov· November 2022

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Advances in gene therapy for neurogenetic diseases: a brief review.
Ying-Xuan Xie, Wen-Qi Lv, Yi-Kun Chen, Shunyan Hong, Xiang-Ping Yao

J Mol Med (Berl)· March 2022

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Base editing-mediated splicing correction therapy for spinal muscular atrophy.
Xiang Lin, Haizhu Chen, Ying-Qian Lu, Shunyan Hong, Xinde Hu

Cell Res· June 2020

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Advances in detecting and reducing off-target effects generated by CRISPR-mediated genome editing.
Jinjing Li, Shunyan Hong, Wanjin Chen, Erwei Zuo, Hui Yang

J Genet Genomics· November 2019

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