Commentary: The mutations and clinical variability in maternally inherited diabetes and deafness: an analysis of 161 patients

Front Endocrinol (Lausanne). 2023 Jun 7:14:1205862. doi: 10.3389/fendo.2023.1205862. eCollection 2023.

Authors

Ivo P van de Peppel^{1

2}, Serwet Demirdas¹, Behiye Özcan³

Affiliations

¹ Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, Netherlands.
² Department of Clinical Genetics, Leiden University Medical Centre, Leiden, Netherlands.
³ Department of Internal Medicine, Erasmus Medical Centre, Rotterdam, Netherlands.

No abstract available

Keywords: MIDD; clinical genetics; diabetes mellitus; heteroplasmy; m.3243A>G; mitochondrial disease.

Publication types

Comment

MeSH terms

Deafness* / genetics
Diabetes Mellitus, Type 2* / genetics
Humans
Mitochondrial Diseases* / genetics
Mutation

Supplementary concepts

Noninsulin-dependent diabetes mellitus with deafness