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Article

The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.

Frontiers in endocrinology - 1 Jan 2021

Yang Mengge, Xu Lusi, Xu Chunmei, Cui Yuying, Jiang Shan, Dong Jianjun, Liao Lin

Abstract excerpt

Aims: To investigate the clinical features and mitochondrial mutations for maternally inherited diabetes and deafness. Methods: PubMed, Embase, Medline, Web of Science, the China National Knowledge Infrastructure, and Wanfang were searched with the following search terms: "Maternally inherited diabetes and deafness" OR "MIDD" OR "Mitochondrial diabetes". The mutations and clinical features were analyzed....

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Deafness

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Share to DNA, Mitochondrial

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Source

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Identifiers

PMID: 34899594
DOI: 10.3389/fendo.2021.728043
PMCID: PMC8654930

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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