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

Frontiers in Endocrinology

Endocrinology

Serwet Demirdas¹  Ivo P. van de Peppel²  Behiye Özcan³ 

[1] Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, Netherlands;Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, Netherlands;Department of Clinical Genetics, Leiden University Medical Centre, Leiden, Netherlands;Department of Internal Medicine, Erasmus Medical Centre, Rotterdam, Netherlands;

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

DOI  :  10.3389/fendo.2023.1205862

 received in 2023-04-14, accepted in 2023-05-29,  发布年份 2023

来源: Frontiers

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