Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations.

CONCLUSION: Although no specific metabolic phenotype could be identified suggesting or eliminating implication of rare mtDNA mutations in diabetes, clinical phenotypes featured more frequent neurological signs.
PMID: 32409007 [PubMed - as supplied by publisher]

Source: Annales d'Endocrinologie - April 27, 2020 Category: Endocrinology Authors: Decoux-Poullot AG, Bannwarth S, Procaccio V, Lebre AS, Jardel C, Vialettes B, Paquis-Flucklinger V, Chevalier N Tags: Ann Endocrinol (Paris) Source Type: research