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6. 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 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
11. A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern. Hosszúfalusi N, Karcagi V, Horváth R, Palik E, Várkonyi J, Rajczy K, Prohászka Z, Szentirmai C, Karádi I, Romics L, Pánczél P. Diabetes Metab Res Rev; 2009 Feb; 25(2):127-35. PubMed ID: 19116951 [Abstract] [Full Text] [Related]
15. [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 17; 145(46):2250-2. PubMed ID: 11757250 [No Abstract] [Full Text] [Related]
19. 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 17; 25(3):370-4. PubMed ID: 18279408 [Abstract] [Full Text] [Related]