Exclusion of adenosine deaminase gene locus on chromosome 20q12–13.1 in familial NIDDM in Taiwanese patients

1. Ooto Y, Nonaka I, Horai S (1990) A mutation in the t R N A LEU(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 348: 651653 2. Tanaka M~ Ino H, Ohbayashi T et al. (1991) Mitochondrial D N A mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Biochem Biophys Res… CONTINUE READING