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

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 diabe...

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Detalles Bibliográficos
Autores principales: Yang, Mengge, Xu, Lusi, Xu, Chunmei, Cui, Yuying, Jiang, Shan, Dong, Jianjun, Liao, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654930/
https://www.ncbi.nlm.nih.gov/pubmed/34899594
http://dx.doi.org/10.3389/fendo.2021.728043

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654930/
https://www.ncbi.nlm.nih.gov/pubmed/34899594
http://dx.doi.org/10.3389/fendo.2021.728043

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