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2. Maternally-inherited diabetes and deafness: report of two affected German families with the A3243G mitochondrial DNA mutation. Thorns C; Widjaja A; Boeck N; Skamira C; Zühlke H Exp Clin Endocrinol Diabetes; 1998; 106(5):384-8. PubMed ID: 9831303 [TBL] [Abstract][Full Text] [Related]
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4. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation. Suzuki S; Hinokio Y; Ohtomo M; Hirai M; Hirai A; Chiba M; Kasuga S; Satoh Y; Akai H; Toyota T Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277 [TBL] [Abstract][Full Text] [Related]
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8. [A new subtype of diabetes mellitus: maternally inherited diabetes and deafness (MIDD)]. Maassen JA; Jansen JJ; van den Ouweland JM; Hart LM; van Essen EH; Lemkes HH Ned Tijdschr Geneeskd; 1998 Jan; 142(5):229-33. PubMed ID: 9557035 [TBL] [Abstract][Full Text] [Related]
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10. [Evolution until death of two members of a family with A3243G mutation and MELAS phenotype versus diabetes mellitus]. Pérez López-Fraile MI; Barrena R; Montoya J; Marta E Neurologia; 2006; 21(6):327-32. PubMed ID: 16799910 [TBL] [Abstract][Full Text] [Related]
11. [Mitochondrial diabetes complicated by or associated with "MELAS" syndrome?]. Drouet A; Guilloton L; Godinot C; Rochet D; Ribot C; Carrier H Rev Neurol (Paris); 2000 Oct; 156(10):892-5. PubMed ID: 11033519 [TBL] [Abstract][Full Text] [Related]
12. Search for mitochondrial DNA mutation at position 3243 in German patients with a positive family history of maternal diabetes mellitus. Klemm T; Neumann S; Trülzsch B; Pistrosch F; Hanefeld M; Paschke R Exp Clin Endocrinol Diabetes; 2001; 109(5):283-7. PubMed ID: 11507652 [TBL] [Abstract][Full Text] [Related]
13. [From gene to disease; mutation in mitochondrial DNA and maternally inherited diabetes mellitus with deafness (MIDD)]. Leys AM; de Jong PT Ned Tijdschr Geneeskd; 2001 Nov; 145(46):2250-2. PubMed ID: 11757250 [No Abstract] [Full Text] [Related]
14. 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]
15. Maternally inherited diabetes and deafness: prevalence in a hospital diabetic population. Newkirk JE; Taylor RW; Howell N; Bindoff LA; Chinnery PF; Alberti KG; Turnbull DM; Walker M Diabet Med; 1997 Jun; 14(6):457-60. PubMed ID: 9212310 [TBL] [Abstract][Full Text] [Related]
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17. A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy. Tabebi M; Mkaouar-Rebai E; Mnif M; Kallabi F; Ben Mahmoud A; Ben Saad W; Charfi N; Keskes-Ammar L; Kamoun H; Abid M; Fakhfakh F Biochem Biophys Res Commun; 2015 Apr; 459(3):353-60. PubMed ID: 25701779 [TBL] [Abstract][Full Text] [Related]
18. Heterogeneous phenotypic manifestations of maternally inherited deafness associated with the mitochondrial A3243G mutation. Case report. Hoptasz M; Szczuciński A; Losy J Neurol Neurochir Pol; 2014; 48(2):150-3. PubMed ID: 24821643 [TBL] [Abstract][Full Text] [Related]