Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.

Diabetic medicine : a journal of the British Diabetic Association - 1 Mar 2008

Katulanda P, Groves C J, Barrett A, Sheriff R, Matthews D R, McCarthy M I, Gloyn A L

Abstract excerpt

AIMS: The maternally inherited mt3243A > G mutation is associated with a variable clinical phenotype including diabetes and deafness (MIDD). We aimed to determine the prevalence and clinical characteristics of MIDD in a large South Asian cohort of young adult-onset diabetic patients from Sri Lanka. METHODS: DNA was available from 994 subjects (age of diagnosis 16-40 years, age at recruitment < or = 45 years)....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Deafness

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diabetes Mellitus

Share to DNA, Mitochondrial

Share to Mutation

Share to Pedigree

Share to Pregnancy

Share to Sri Lanka

Source

Identifiers

PMID: 18279408
DOI: 10.1111/j.1464-5491.2007.02377.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka.PMID 18279408Read ↗

Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.Semantic proximity Read ↗

The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.Semantic proximity Read ↗

A review of maternally inherited diabetes and deafness.Semantic proximity Read ↗

Diabetes Associated With Maternally Inherited Diabetes and Deafness (MIDD): From Pathogenic Variant to Phenotype.Semantic proximity Read ↗

Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population.Semantic proximity Read ↗

Maternally Inherited Diabetes and Deafness (MIDD) - a Series of Case ReportsSemantic proximity Read ↗

Screening for Maternally Inherited Diabetes and Deafness in Large Cohorts of Hearing Impaired and Diabetic Patients.Semantic proximity Read ↗

Screening for Maternally Inherited Diabetes and Deafness in Large Cohorts of Hearing Impaired and Diabetic PatientsSemantic proximity Read ↗

[Mitochondrial diabetes: clinical features, diagnosis and management].Semantic proximity Read ↗

Clinical and Genetic Characteristics and Outcome in Patients with Neonatal Diabetes Mellitus from a Low Middle-income CountrySemantic proximity Read ↗

Clinical Characteristics of Diabetes in People with Mitochondrial DNA 3243A>G Mutation in Korea.Semantic proximity Read ↗

Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.