Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.

Leber's Hereditary Optic Neuropathy with Mitochondrial DNA Mutation G11778A: A Systematic Literature Review and Meta-Analysis.

Jiajia Yuan, Jiaxun Zhao,Chong Ye,Long Pang,Xin Zhang,Alvin Luk,Yangyang Du,Kai Yoon Fan,Xiaowen Zhang,Bin Li,Changzheng Chen

BioMed research international（2023）

Cited 0|Views8
No score
Abstract
The G11778A mutation is a prevalent mitochondrial DNA mutation accounting for over half of LHON cases with three primary mutations. Spontaneous visual recovery is rare, and no effective treatment is currently available.
More
Translated text
Key words
hereditary optic neuropathy,mitochondrial dna mutation g11778a,lebers,meta-analysis
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined