Lack of association between mitochondrial DNA mutation np3243 and maternally inherited diabetes mellitus

Clinical Biochemistry

Volumn 32, Issue 1, 1999, Pages 81-82

  Zambelli, Andrés ^a   Vidal Rioja, Lidia ^a  

^a Instituto Multidisciplinario de Biologia Celular   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

DIABETES MELLITUS; DNA FLANKING REGION; FIBROBLAST; GENE DUPLICATION; GENE MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; QUANTITATIVE ASSAY; SCREENING; SHORT SURVEY; VERTICAL TRANSMISSION;

EID: 0033014171     PISSN: 00099120     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-9120(98)00102-7     Document Type: Article

References (6)

1. Gerbitz K.-D., van den Ouweland J.M.W., Maassen J.A., Jaksch M. Mitochondrial diabetes mellitus a review . Biochim Biophys Acta. 1271:1995;253-260.
2. leu(UUR) gene. Diabetes. 43:1994;746-751.
3. leu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nature Genet. 1:1992;368-371.
4. Ballinger S.W., Shoffner J.M., Gebhart S., et al. Mitochondrial diabetes revisited. Nature Genet. 7:1994;458-459.
5. Gebhart S., Shoffner J.M., Koontz D., et al. Insulin resistance associated with maternally inherited diabetes and deafness. Metabolism. 45:1996;526-531.
6. Suzuki Y., Suzuki S., Hinokio Y., et al. Diabetes associated with a novel mitochondrial tRNA(leu(UUR) mutation. Diabetes Care. 20:1997;1138-1140.