Renal complications in patients with diabetes mellitus associated with an A to G mutation of mitochondrial DNA at the 3243 position of leucine tRNA
- 1 June 1999
- journal article
- case report
- Published by Elsevier in Diabetes Research and Clinical Practice
- Vol. 44 (3) , 183-189
- https://doi.org/10.1016/s0168-8227(99)00051-0
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- The kidney in mitochondrial cytopathiesKidney International, 1997
- The high prevalence of the diabetic patients with a mutation in the mitochondrial gene in JapanJournal of Clinical Endocrinology & Metabolism, 1994
- Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNALEU(UUR) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)Diabetologia, 1994
- A Subtype of Diabetes Mellitus Associated with a Mutation of Mitochondrial DNANew England Journal of Medicine, 1994
- Mitochondrial tRNAlle mutation in fatal cardiomyopathyBiochemical and Biophysical Research Communications, 1992
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Kearns‐Sayre syndrome presenting as renal tubular acidosisNeurology, 1990
- Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)Journal of the Neurological Sciences, 1989
- Pathogenesis and Significance of Nonprimary Focal and Segmental GlomerulosclerosisAmerican Journal of Kidney Diseases, 1989
- Mitochondrial myopathiesAnnals of Neurology, 1985