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Mitochondrial diabetes: molecular mechanisms and clinical presentation

Mitochondrial diabetes: molecular mechanisms and clinical presentation

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_80126596

Mitochondrial diabetes: molecular mechanisms and clinical presentation

About this item

Full title

Mitochondrial diabetes: molecular mechanisms and clinical presentation

Publisher

United States: American Diabetes Association

Journal title

Diabetes (New York, N.Y.), 2004-02, Vol.53 Suppl 1 (2), p.S103-S109

Language

English

Formats

Publication information

Publisher

United States: American Diabetes Association

More information

Scope and Contents

Contents

Mutations in mitochondrial DNA (mtDNA) associate with various disease states. A few mtDNA mutations strongly associate with diabetes, with the most common mutation being the A3243G mutation in the mitochondrial DNA-encoded tRNA(Leu,UUR) gene. This article describes clinical characteristics of mitochondrial diabetes and its molecular diagnosis. Furt...

Alternative Titles

Full title

Mitochondrial diabetes: molecular mechanisms and clinical presentation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_80126596

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_80126596

Other Identifiers

ISSN

0012-1797

E-ISSN

1939-327X

DOI

10.2337/diabetes.53.2007.s103

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