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Journal Abstract Search

180 related items for PubMed ID: 11175301

  • 1. Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutation.
    Hutchin TP, Lench NJ, Arbuzova S, Markham AF, Mueller RF.
    Eur J Hum Genet; 2001 Jan; 9(1):56-8. PubMed ID: 11175301
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  • 3. Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.
    Chapiro E, Feldmann D, Denoyelle F, Sternberg D, Jardel C, Eliot MM, Bouccara D, Weil D, Garabédian EN, Couderc R, Petit C, Marlin S.
    Eur J Hum Genet; 2002 Dec; 10(12):851-6. PubMed ID: 12461693
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  • 4. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature.
    Berrettini S, Forli F, Passetti S, Rocchi A, Pollina L, Cecchetti D, Mancuso M, Siciliano G.
    Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147
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  • 5. Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
    Verhoeven K, Ensink RJ, Tiranti V, Huygen PL, Johnson DF, Schatteman I, Van Laer L, Verstreken M, Van de Heyning P, Fischel-Ghodsian N, Zeviani M, Cremers CW, Willems PJ, Van Camp G.
    Eur J Hum Genet; 1999 Jan; 7(1):45-51. PubMed ID: 10094190
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  • 6. Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness.
    Sevior KB, Hatamochi A, Stewart IA, Bykhovskaya Y, Allen-Powell DR, Fischel-Ghodsian N, Maw MA.
    Am J Med Genet; 1998 Jan 13; 75(2):179-85. PubMed ID: 9450881
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  • 7. Hearing loss due to the mitochondrial A1555G mutation in Italian families.
    Casano RA, Bykhovskaya Y, Johnson DF, Hamon M, Torricelli F, Bigozzi M, Fischel-Ghodsian N.
    Am J Med Genet; 1998 Oct 12; 79(5):388-91. PubMed ID: 9779807
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  • 8. 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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  • 10. Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families.
    Wu CC, Chiu YH, Chen PJ, Hsu CJ.
    Ear Hear; 2007 Jun 01; 28(3):332-42. PubMed ID: 17485982
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  • 11. Sequence analysis of the mitochondrial genome from a large family with maternally inherited nonsyndromic deafness.
    Zhang HJ, Xu CH, Zhan YJ, Zhao SY, Shan YF, Geng XX, Shan XN.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug 01; 22(4):368-71. PubMed ID: 16086269
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  • 13. Biochemical characterization of the deafness-associated mitochondrial tRNASer(UCN) A7445G mutation in osteosarcoma cell cybrids.
    Li X, Zhang LS, Fischel-Ghodsian N, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 11; 328(2):491-8. PubMed ID: 15694374
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  • 15. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.
    Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2005 Oct 28; 336(3):967-73. PubMed ID: 16168391
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  • 17. Mitochondrial deafness.
    Kokotas H, Petersen MB, Willems PJ.
    Clin Genet; 2007 May 28; 71(5):379-91. PubMed ID: 17489842
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  • 18. Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment.
    Lehtonen MS, Uimonen S, Hassinen IE, Majamaa K.
    Eur J Hum Genet; 2000 Apr 28; 8(4):315-8. PubMed ID: 10854117
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