Mitochondrial Diabetes: The Clinical Spectrum of MIDD and MELAS in Association With the A3243G Mutation
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DOI: 10.1210/jendso/bvab048.799
Abstract: Introduction: Maternally inherited diabetes and deafness (MIDD) is a multisystem disorder characterized by insulinopenia and sensorineural hearing loss. This rare form of monogenic diabetes is most commonly associated with the A3243G mutation of mitochondrial DNA… read more here.
Keywords: midd melas; patient; a3243g mutation; midd ... See more keywords