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4. Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy? Holmes-Walker DJ; Mitchell P; Boyages SC Diabet Med; 1998 Nov; 15(11):946-52. PubMed ID: 9827849 [TBL] [Abstract][Full Text] [Related]
5. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation. Smith PR; Bain SC; Good PA; Hattersley AT; Barnett AH; Gibson JM; Dodson PM Ophthalmology; 1999 Jun; 106(6):1101-8. PubMed ID: 10366077 [TBL] [Abstract][Full Text] [Related]
6. Screening of patients with maternally transmitted diabetes for mitochondrial gene mutations in the tRNA[Leu(UUR)] region. Tsukuda K; Suzuki Y; Kameoka K; Osawa N; Goto Y; Katagiri H; Asano T; Yazaki Y; Oka Y Diabet Med; 1997 Dec; 14(12):1032-7. PubMed ID: 9455930 [TBL] [Abstract][Full Text] [Related]
7. Mitochondrial 3243 BP mutation: a case report. Rigoli L; Caruso RA; Zuccarello D; Rigoli M; Barberi I Diabetes Nutr Metab; 2001 Dec; 14(6):343-8. PubMed ID: 11853367 [TBL] [Abstract][Full Text] [Related]
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9. Prevalence and clinical characteristics of maternally inherited diabetes and deafness caused by the mt3243A > G mutation in young adult diabetic subjects in Sri Lanka. Katulanda P; Groves CJ; Barrett A; Sheriff R; Matthews DR; McCarthy MI; Gloyn AL Diabet Med; 2008 Mar; 25(3):370-4. PubMed ID: 18279408 [TBL] [Abstract][Full Text] [Related]
10. Mutation in mitochondrial tRNA(Leu)(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. van den Ouweland JM; Lemkes HH; Ruitenbeek W; Sandkuijl LA; de Vijlder MF; Struyvenberg PA; van de Kamp JJ; Maassen JA Nat Genet; 1992 Aug; 1(5):368-71. PubMed ID: 1284550 [TBL] [Abstract][Full Text] [Related]
11. [Clinical characterizations of familial diabetes mellitus associated with mitochondrial gene mutation]. Xiu L; Zhang Q; Yu B Zhonghua Yi Xue Za Zhi; 1997 Jun; 77(6):418-21. PubMed ID: 9772504 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome. Perucca-Lostanlen D; Narbonne H; Hernandez JB; Staccini P; Saunieres A; Paquis-Flucklinger V; Vialettes B; Desnuelle C Biochem Biophys Res Commun; 2000 Nov; 277(3):771-5. PubMed ID: 11062027 [TBL] [Abstract][Full Text] [Related]
13. Maternally inherited diabetes and deafness: a diabetic subtype associated with a mutation in mitochondrial DNA. Maassen JA; van den Ouweland JM; t Hart LM; Lemkes HH Horm Metab Res; 1997 Feb; 29(2):50-5. PubMed ID: 9105898 [TBL] [Abstract][Full Text] [Related]
14. 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. van den Ouweland JM; Lemkes HH; Trembath RC; Ross R; Velho G; Cohen D; Froguel P; Maassen JA Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800 [TBL] [Abstract][Full Text] [Related]
15. Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu)(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease. van den Ouweland JM; Maechler P; Wollheim CB; Attardi G; Maassen JA Diabetologia; 1999 Apr; 42(4):485-92. PubMed ID: 10230654 [TBL] [Abstract][Full Text] [Related]
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19. Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation. van den Ouweland JM; Lemkes HH; Gerbitz KD; Maassen JA Muscle Nerve Suppl; 1995; 3():S124-30. PubMed ID: 7603513 [TBL] [Abstract][Full Text] [Related]
20. Novel mitochondrial DNA mutation in tRNA(Lys) (8296A-->G) associated with diabetes. Kameoka K; Isotani H; Tanaka K; Azukari K; Fujimura Y; Shiota Y; Sasaki E; Majima M; Furukawa K; Haginomori S; Kitaoka H; Ohsawa N Biochem Biophys Res Commun; 1998 Apr; 245(2):523-7. PubMed ID: 9571188 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]