Chenghui Wang
Yiwu, China
Last Updated: 09/26/2026
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Found 8 publications
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy.
Journal: Human molecular genetics
Published: July 11, 2022
OPA1 haploinsufficiency due to a novel splicing variant resulting in mitochondrial dysfunction without mitochondrial DNA depletion.
Journal: Ophthalmic genetics
Published: November 30, 2020
An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal function.
Journal: The Journal of biological chemistry
Published: September 09, 2020
PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.
Journal: The Journal of clinical investigation
Published: November 14, 2019
Overexpression of human mitochondrial alanyl-tRNA synthetase suppresses biochemical defects of the mt-tRNAAla mutation in cybrids.
Journal: International journal of biological sciences
Published: May 03, 2018
Mutation analysis of Leber's hereditary optic neuropathy using a multi-gene panel.
Journal: Biomedical reports
Published: August 10, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026