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Article

A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene.

Muscle & nerve. Supplement - 1 Jan 1995

Kadowaki T, Sakura H, Otabe S, Yasuda K, Kadowaki H, Mori Y, Hagura R, Akanuma Y, Yazaki Y

Abstract excerpt

Recently, in patients with diabetes and deafness, researchers have identified an A to G transition at position 3243 in transfer ribonucleic acid(Leu)(UUR) [3243 base-pair (bp) mutation], originally found in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike epis...

Topics

Adult
Base Sequence
DNA, Mitochondrial
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Female
Genes
Humans
Insulin
Insulin Secretion
Male
Middle Aged
Molecular Sequence Data

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Mutation

RNA, Transfer, Leu

Source

Identifiers

PMID: 7603515
DOI: 10.1002/mus.880181427

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7603515-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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