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....
Topics
- Biological Variation, Population
- Cohort Studies
- DNA, Mitochondrial
- Deafness
- Diabetes Mellitus, Type 2
- Genetic Heterogeneity
- Humans
- Infant, Newborn
- Mitochondrial Diseases
- Mutation
- Phenotype