Article info
PDFNeurogenetics
Original research
Frameshift mutation of Timm8a1 gene in mouse leads to an abnormal mitochondrial structure in the brain, correlating with hearing and memory impairment
- Correspondence to Professor Yafang Hu, Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China; yafanghu{at}smu.edu.cn
Citation
Frameshift mutation of Timm8a1 gene in mouse leads to an abnormal mitochondrial structure in the brain, correlating with hearing and memory impairment
Publication history
- Received March 5, 2020
- Revised June 12, 2020
- Accepted July 5, 2020
- First published August 20, 2020.
Online issue publication
January 08, 2022
Article Versions
- Previous version (8 January 2022).
- You are viewing the most recent version of this article.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.