6Ohkubo K, Yamano A, Nagashima N, et al. Mitochondrial gene mutations in the tRNA^Leu(UUR) region and diabetes: prevalence and clinical phenotypes in Japan[J]. Clinical Chemistry, 2001, 47 (12) : 1641-1648.
7Kadowaki T, Kadowaki H, Mori Y, et al. A subtype of diabetes mellitus associated with a mutation of mitoehondrial DNA[J]. N Engl J Med,1994,330(14) :962-968.
9Janssen GM,Maassen JA,van den Ouweland JM. The diabetes- associated 3243 mutation in the mitochondrial tRNA^Leu(UUR) gene causes severe mitochondrial dysfunction without a strong decrease in protein synthesis rate[J]. J Biol Chem, 1999,274 (42) :29744-29748.
10Chomyn A, Enriquez JA, Micol V, et al. The mitochondrial myopathy, eneephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitoehondrial tRNA^Leu(UUR) mutation causes amlnoacylatlon deficiency and concomitant reduced association of mRNA with ribosornes[J]. J Biol Chem,2000,275(25) : 19198-19209.
6Xiang KS, Wang YQ, Wu SH, et al. Mitoehondrial tRNA^Leu(UUR) gene mutation diabetes mellitus in Chinese. Chin Med J (Engl),1997, 110:372-378.
7Linnane AW, Marzuki S, Ozawa T, et al. Mitochondrial DNA mutations as an important contributor to ageing and degenerative disease. Lancet, 1989,1 : 642-645.
8Kadowaki H, Tobe K, Mori Y, et al. Mitochondrial gene mutation and insulin-deficient type of diabetes mellitus. Lancet, 1993, 341 : 893.
9Suzuki S. Diabetes mellitus with mitochondrial gene mutations in Japan. Ann N YAcad Sci, 2004,1011 : 185-192.