The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10‐year follow‐up observation study and literature review

Key Clinical Message Maternally inherited diabetes and deafness (MIDD) is often caused by the m.3243A > G mutation in mitochondrial DNA. Unfortunately, the characteristics of MIDD, especially long‐term outcomes and heteroplasmic changes, have not been well described previously. The purpose of this s...

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Hlavní autoři:	Shasha Zheng, Juanjuan Wang, Minxian Sun, Pei Wang, Wei Shi, Zhongzhi Zhang, Zhongjing Wang, Hongmei Zhang
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Wiley 2024-02-01
Edice:	Clinical Case Reports
Témata:	clinical features diagnosis genetic testing m.3243A > G mutation maternally inherited diabetes and deafness (MIDD) mitochondrial genes
On-line přístup:	https://doi.org/10.1002/ccr3.8458
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