Publication:
Mitochondrial Diabetes A Rare Case

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorSingh, Arun Kumar
dc.contributor.authorMsasko, Aoki
dc.contributor.authorMiyata, Midori
dc.contributor.authorMine, Yasuke
dc.contributor.authorSuzuki, Junichi
dc.contributor.authorUrakami, Tatsuhiko
dc.date.accessioned2026-02-04T05:09:00Z
dc.date.available2026-02-04T05:09:00Z
dc.date.issued2017
dc.descriptionArun Kumar Singh B.P.Koirala Institute of Health Sciences Aoki Msasko Department of Paediatrics, Nihon University Hospital,Tokyo Midori Miyata Department of Paediatrics, Nihon University Hospital,Tokyo Yasuke Mine Department of Paediatrics, Nihon University Hospital,Tokyo Junichi Suzuki Department of Paediatrics, Nihon University Hospital,Tokyo Tatsuhiko Urakami Department of Paediatrics, Nihon University Hospital,Tokyo
dc.description.abstractAbstract: A 25 years female diagnosed and confirmed mitochondrial by gene analysis mutation DNA 3243(A-G). CQ10 was useful for the resolution of clinical symptoms, and metformin should be avoided in mito-chondrial diabetes.
dc.identifierhttps://doi.org/10.3126/jnps.v37i3.18765
dc.identifier.urihttps://hdl.handle.net/20.500.14572/4489
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectMitochondrial diabetes
dc.subjectMetformin
dc.subjectWolff-Parkinson-White (WPW) syndrome
dc.titleMitochondrial Diabetes A Rare Case
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage292
oaire.citation.startPage290
relation.isJournalIssueOfPublication97340c14-0d1f-4808-806c-8504b2e33439
relation.isJournalIssueOfPublication.latestForDiscovery97340c14-0d1f-4808-806c-8504b2e33439
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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