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Journal Abstract Search

423 related items for PubMed ID: 25701779

  • 1. 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 10; 459(3):353-60. PubMed ID: 25701779
    [Abstract] [Full Text] [Related]

  • 2. Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation.
    Tabebi M, Charfi N, Kallabi F, Alila-Fersi O, Ben Mahmoud A, Tlili A, Keskes-Ammar L, Kamoun H, Abid M, Mnif M, Fakhfakh F.
    J Diabetes Complications; 2017 Jan 10; 31(1):253-259. PubMed ID: 27422531
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  • 3. A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions.
    Mezghani N, Mnif M, Mkaouar-Rebai E, Kallel N, Charfi N, Abid M, Fakhfakh F.
    Biochem Biophys Res Commun; 2013 Feb 22; 431(4):670-4. PubMed ID: 23357420
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  • 4. A novel mitochondrial DNA missense mutation at G3421A in a family with maternally inherited diabetes and deafness.
    Chen FL, Liu Y, Song XY, Hu HY, Xu HB, Zhang XM, Shi JH, Hu J, Shen Y, Lu B, Wang XC, Hu RM.
    Mutat Res; 2006 Dec 01; 602(1-2):26-33. PubMed ID: 16949108
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  • 5. A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual loss.
    Mkaouar-Rebai E, Chamkha I, Kammoun T, Alila-Fersi O, Aloulou H, Hachicha M, Fakhfakh F.
    Biochem Biophys Res Commun; 2013 Jan 11; 430(2):585-91. PubMed ID: 23219819
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  • 6. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.
    Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC.
    Nat Genet; 1992 Apr 11; 1(1):11-5. PubMed ID: 1301992
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  • 7. The heteroplasmic m.14709T>C mutation in the tRNA(Glu) gene in two Tunisian families with mitochondrial diabetes.
    Mezghani N, Mkaouar-Rebai E, Mnif M, Charfi N, Rekik N, Youssef S, Abid M, Fakhfakh F.
    J Diabetes Complications; 2010 Apr 11; 24(4):270-7. PubMed ID: 20045353
    [Abstract] [Full Text] [Related]

  • 8. Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.
    Ma L, Wang H, Chen J, Jin W, Liu L, Ban B, Shen J, Hua Z, Chai J.
    Chin Med J (Engl); 2000 Feb 11; 113(2):111-6. PubMed ID: 11775531
    [Abstract] [Full Text] [Related]

  • 9. A novel mutation in mitochondrial DNA in a patient with diabetes, deafness and proteinuria.
    Adema AY, Janssen MC, van der Heijden JW.
    Neth J Med; 2016 Dec 11; 74(10):455-457. PubMed ID: 27966441
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  • 11. Maternally inherited diabetes and deafness (MIDD): unusual occult exocrine pancreatic manifestation in an affected German family.
    Schleiffer T, 't Hart LM, Schürfeld C, Kraatz K, Riemann JF.
    Exp Clin Endocrinol Diabetes; 2000 Dec 11; 108(2):81-5. PubMed ID: 10826513
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  • 13. 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 11; 1(5):368-71. PubMed ID: 1284550
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  • 15. [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 31; 142(5):229-33. PubMed ID: 9557035
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