Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family
- 1 April 2001
- journal article
- research article
- Published by Wiley in Diabetic Medicine
- Vol. 18 (4) , 334-336
- https://doi.org/10.1046/j.1464-5491.2001.00429-2.x
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
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- Mitochondrial DNA Mutations and PathogenesisJournal of Bioenergetics and Biomembranes, 1997
- Maternally Inherited Diabetes Mellitus: the Role of Mitochondrial DNA DefectsDiabetic Medicine, 1995
- Complete mtDNA sequence of a patient in a maternal pedigree with sensorineruar deatinessHuman Molecular Genetics, 1994
- Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) geneFEBS Letters, 1993