DNM1L-Related Mitochondrial Fission Defects Presenting as Encephalopathy: A Case Report and Literature Review
Background: Mitochondrial dynamics, including mitochondrial fission and fusion, transport and distribution, biogenesis and degradation, are critical to neuronal function. The dynamin-1 like (DNM1L) gene encodes dynamin-related protein 1 (DRP1/DLP1), which is an evolutionarily conserved member of the...
Saved in:
Main Authors: | Xingmiao Liu (Author), Zhongbin Zhang (Author), Dong Li (Author), Meifang Lei (Author), Qing Li (Author), Xiaojun Liu (Author), Peiyuan Zhang (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2021-07-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Truncated DNM1 variant underlines developmental delay and epileptic encephalopathy
by: Tayyaba Afsar, et al.
Published: (2023) -
Protective Effects of Inhibition of Mitochondrial Fission on Organ Function After Sepsis
by: Yu Zhu, et al.
Published: (2021) -
Mitochondrial Fission as a Therapeutic Target for Metabolic Diseases: Insights into Antioxidant Strategies
by: Tianzheng Yu, et al.
Published: (2023) -
Corrigendum: Protective effects of inhibition of mitochondrial fission on organ function after sepsis
by: Yu Zhu, et al.
Published: (2024) -
Overproduction of Mitochondrial Fission Proteins in Membranous Nephropathy in Children
by: Qi-Jiao Wei, et al.
Published: (2018)