Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients
Main Authors: | Ivo P. van de Peppel, Serwet Demirdas, Behiye Özcan |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2023-06-01
|
Series: | Frontiers in Endocrinology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fendo.2023.1205862/full |
Similar Items
-
Maternally inherited diabetes mellitus and deafness (MIDD): A case report and review of literature
by: Prabhat K Agrawal, et al.
Published: (2023-01-01) -
The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10‐year follow‐up observation study and literature review
by: Shasha Zheng, et al.
Published: (2024-02-01) -
Impaired Nuclear and Mitochondrial Cross-Talk Might Alter mtDNA Epigenetic Regulation in Maternally Inherited Diabetes- and Deafness-Affected Patients
by: Luigi Donato, et al.
Published: (2023-03-01) -
Pathogenic mitochondrial DNA 3243A>G mutation: From genetics to phenotype
by: Danyang Li, et al.
Published: (2022-10-01) -
Changes in histopathology and heteroplasmy rates over 8 years and effectiveness of taurine supplementation in a patient with mitochondrial nephropathy caused by MT-TL1 mutation: A case report
by: Toshiyuki Imasawa, et al.
Published: (2023-04-01)