Mitochondrial diabetes mellitus: a review
- 24 May 1995
- journal article
- review article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
- Vol. 1271 (1), 253-260
- https://doi.org/10.1016/0925-4439(95)00036-4
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Prevalence of mitochondrial gene mutations in families with diabetes mellitusThe Lancet, 1993
- Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabeticsThe Lancet, 1993
- Japanese case of diabetes mellitus and . deafness with mutation in mitochondrial tRNALeu(UUR)geneThe Lancet, 1993
- Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) geneFEBS Letters, 1993
- Glucokinase-defective NIDDMThe Lancet, 1993
- Mitochondrial gene mutations and diabetes mellitusThe Lancet, 1993
- Pearson bone marrow-pancreas syndrome with insulin-dependent diabetes, progressive renal tubulopathy, organic aciduria and elevated fetal haemoglobin caused by deletion and duplication of mitochondrial DNAEuropean Journal of Pediatrics, 1993
- Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNAThe Lancet, 1992
- An ND-6 mitochondrial DNA mutation associated with leber hereditary optic neuropathyBiochemical and Biophysical Research Communications, 1992
- Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletionNature Genetics, 1992