A novel homozygous variant in MICOS13/QIL1 causes hepato‐encephalopathy with mitochondrial DNA depletion syndrome
Abstract Background Mitochondrial DNA depletion syndrome (MTDPS) is part of a group of mitochondrial diseases characterized by a reduction in mitochondrial DNA copy number. Most MTDPS is caused by mutations in genes that disrupt deoxyribonucleotide metabolism. Methods We performed the whole‐exome se...
Main Authors: | Yoshihito Kishita, Masaru Shimura, Masakazu Kohda, Masumi Akita, Atsuko Imai‐Okazaki, Yukiko Yatsuka, Yoko Nakajima, Tetsuya Ito, Akira Ohtake, Kei Murayama, Yasushi Okazaki |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2020-10-01
|
Series: | Molecular Genetics & Genomic Medicine |
Subjects: | |
Online Access: | https://doi.org/10.1002/mgg3.1427 |
Similar Items
-
Emerging Roles of the MICOS Complex in Cristae Dynamics and Biogenesis
by: Ruchika Anand, et al.
Published: (2021-06-01) -
QIL1 mutation causes MICOS disassembly and early onset fatal mitochondrial encephalopathy with liver disease
by: Virginia Guarani, et al.
Published: (2016-09-01) -
MICOS coordinates with respiratory complexes and lipids to establish mitochondrial inner membrane architecture
by: Jonathan R Friedman, et al.
Published: (2015-04-01) -
Successful Diagnosis of Sengers Syndrome Using a Comprehensive Genomic Analysis
by: Kohta Nakamura, et al.
Published: (2025-01-01) -
Pathways shaping the mitochondrial inner membrane
by: Till Klecker, et al.
Published: (2021-12-01)