SPG7 (paraplegin) and the mitochondrial permeability transition pore
Main Authors: | Paolo eBernardi, Michael eForte |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2015-11-01
|
Series: | Frontiers in Physiology |
Subjects: | |
Online Access: | http://journal.frontiersin.org/Journal/10.3389/fphys.2015.00320/full |
Similar Items
-
Impaired flickering of the permeability transition pore causes SPG7 spastic paraplegia
by: Irene Sambri, et al.
Published: (2020-11-01) -
Mitochondrial Function in Hereditary Spastic Paraplegia: Deficits in SPG7 but Not SPAST Patient-Derived Stem Cells
by: Gautam Wali, et al.
Published: (2020-08-01) -
The mitochondrial permeability transition pore: A mystery solved?
by: Paolo eBernardi, et al.
Published: (2013-05-01) -
Identification of novel compound heterozygous SPG7 mutations-related hereditary spastic paraplegia in a Chinese family: a case report
by: Xiaoqian Zhang, et al.
Published: (2018-11-01) -
A Comprehensive In Silico Analysis of Deleterious SNPs of Paraplegin Protein Associated with Hereditary Spastic Paraplegia through Mitochondrial Dysfunction
by: Ammara Akhtar, et al.
Published: (2020-06-01)