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Journal Abstract Search

219 related items for PubMed ID: 21994425

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  • 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; 31(1):253-259. PubMed ID: 27422531
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  • 6. 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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  • 8. 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 22; 74(10):455-457. PubMed ID: 27966441
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  • 9. The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.
    Yang M, Xu L, Xu C, Cui Y, Jiang S, Dong J, Liao L.
    Front Endocrinol (Lausanne); 2021 Dec 22; 12():728043. PubMed ID: 34899594
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  • 15. Late onset of type 2 diabetes is associated with mitochondrial tRNATrp A5514G and tRNASer(AGY) C12237T mutations.
    Yang L, Guo Q, Leng J, Wang K, Ding Y.
    J Clin Lab Anal; 2022 Jan 22; 36(1):e24102. PubMed ID: 34811812
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  • 16. Mitochondrial diabetes in children: seek and you will find it.
    Mazzaccara C, Iafusco D, Liguori R, Ferrigno M, Galderisi A, Vitale D, Simonelli F, Landolfo P, Prisco F, Masullo M, Sacchetti L.
    PLoS One; 2012 Jan 22; 7(4):e34956. PubMed ID: 22536343
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  • 17. Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness.
    Perucca-Lostanlen D, Taylor RW, Narbonne H, Mousson de Camaret B, Hayes CM, Saunieres A, Paquis-Flucklinger V, Turnbull DM, Vialettes B, Desnuelle C.
    Biochim Biophys Acta; 2002 Dec 12; 1588(3):210-6. PubMed ID: 12393175
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  • 18. Variants m.13276G>A in the MT-ND5 and m.8241T>G in the MT-CO2 gene are not responsible for maternally inherited diabetes and deafness.
    Finsterer J, Zarrouk-Mahjoub S.
    J Diabetes Complications; 2017 Nov 12; 31(11):1638. PubMed ID: 28890306
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  • 19. The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes.
    Laloi-Michelin M, Meas T, Ambonville C, Bellanné-Chantelot C, Beaufils S, Massin P, Vialettes B, Gin H, Timsit J, Bauduceau B, Bernard L, Bertin E, Blickle JF, Cahen-Varsaux J, Cailleba A, Casanova S, Cathebras P, Charpentier G, Chedin P, Crea T, Delemer B, Dubois-Laforgue D, Duchemin F, Ducluzeau PH, Bouhanick B, Dusselier L, Gabreau T, Grimaldi A, Guerci B, Jacquin V, Kaloustian E, Larger E, Lecleire-Collet A, Lorenzini F, Louis J, Mausset J, Murat A, Nadler-Fluteau S, Olivier F, Paquis-Flucklinger V, Paris-Bockel D, Raynaud I, Reznik Y, Riveline JP, Schneebeli S, Sonnet E, Sola-Gazagnes A, Thomas JL, Trabulsi B, Virally M, Guillausseau PJ, Mitochondrial Diabetes French Study Group.
    J Clin Endocrinol Metab; 2009 Aug 12; 94(8):3025-30. PubMed ID: 19470619
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