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1. van den Ouweland JMW, Lemkes HHPJ, Ruitenbeek W et al. (1992) Mutation in the mitochondrial tRNA LEU(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet 1: 368±371 2. Katagiri H, Asano T, Ishihara H et al. (1994) Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA (Leu(UU 11) ) gene mutation in Japanese patients. Diabetologia 37: 504±510 3. Kishimoto M, Hashiramoto M, Araki S et al. (1995) Diabetes mellitus carrying a mutation in the mitochondrial tRNA (Leu(UUR) ) gene. Diabetologia 38: 193±200 4. Tsukuda K, Suzuki Y, Kameoka K et al. (1997) Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNALeu(UUR) region. Diabet Med 14: 1032±1037 5. Larsson NG, Tulinus MH, Holme E et al. (1992) Segregation and manifestations of the tRNA lys A-G (8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome. Am J Hum Genet 51: 1201±1212 6. Olsson C, Zethelius B, Lagerstrom-Fermer M et al. (1998) Level of heteroplasmy for the mitochondrial mutation A3243 G correlate with age at onset of diabetes and deafness. Hum Mutat 12: 52±58 7. 't Hart LM, Jansen JJ, Lemkes HHPJ et al. (1996) Heteroplasmy levels of a mitochondrial gene mutation associated with diabetes mellitus decrease in leucocyte DNA upon aging. Hum Mutat 7: 193±197

Autoantibodies to human tissue transgutaminase identify silent coeliac disease in Type I diabetes