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International Journal of Diabetes Mellitus
Volume 2, Issue 1
, Page 69
, April 2010
Mitochondrial tRNALeu(UUR) gene mutation and maternally inherited diabetes mellitus in Pakistan population
References
- . Mitochondrial tRNALeu(UUR) gene mutation and maternally inherited diabetes mellitus in Pakistan population. Int J Diabetes Mellitus. 2009;1:11–15
- . Prevalence of diabetes in Pakistan. Diabetes Res Clin Practice. 2007;76:219–222
- Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness. J Med Genet. 1995;32:654–656
- Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene. Diabetes. 1994;43:746–751
- Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation. Ophthalmology. 1999;106:1101–1108
PII: S1877-5934(09)00064-2
doi: 10.1016/j.ijdm.2009.12.007
© 2009 International Journal of Diabetes Mellitus. Published by Elsevier Inc. All rights reserved.
« Previous
International Journal of Diabetes Mellitus
Volume 2, Issue 1
, Page 69
, April 2010
