Multi-mtDNA Variants May Be a Factor Contributing to Mitochondrial Function Variety in the Skin-Derived Fibroblasts of Leber's Hereditary Optic Neuropathy Patients
Heterogeneity is a major feature of Leber's hereditary optic neuropathy (LHON) and has a significant impact on the manifestation and diagnosis of the disease. This study explored whether multiple variations in mitochondrial genes were associated with the heterogeneity, mainly phenotypic heterog...
Main Authors: | Shun Yao, Qingru Zhou, Mingzhu Yang, Ya Li, Xiuxiu Jin, Qingge Guo, Lin Yang, Fangyuan Qin, Bo Lei |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-07-01
|
Series: | Frontiers in Molecular Neuroscience |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fnmol.2022.920221/full |
Similar Items
-
Superoxide dismutase 2 ameliorates mitochondrial dysfunction in skin fibroblasts of Leber’s hereditary optic neuropathy patients
by: Qingru Zhou, et al.
Published: (2022-08-01) -
The Genetics of Leber’s Hereditary Optic Neuropathy: A Literature Review
by: Henry Liu
Published: (2018-11-01) -
La neuropatia ottica ereditaria di Leber (Leber Hereditary Optic Neuropathy, LHON)
by: Maria Lucia Cascavilla
Published: (2017-02-01) -
Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber’s Hereditary Optic Neuropathy (LHON) Subjects
by: Mirko Baglivo, et al.
Published: (2023-08-01) -
Increased protein S-glutathionylation in Leber’s hereditary optic neuropathy (LHON)
by: Zhou, Lei, et al.
Published: (2021)