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Journal Abstract Search

370 related items for PubMed ID: 16631122

  • 41. [Nonsyndromic inherited hearing impairment caused by mtDNA double mutations of A1555G and 961 insC].
    Cao X, Xing GQ, Wei QJ, Bu XK, Wang DY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):629-32. PubMed ID: 15583999
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  • 45. [Epidemiological studies on mtDNA 12S rRNA A1555G mutation of 10 non syndromic hearing loss families in Yunnan province].
    Ma T, Xue X, Dai P, Cao X, Chi J, Deng J, Pang K, Liu W.
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Jul; 26(13):581-5. PubMed ID: 23002640
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  • 46. Rapid identification of an A1555G mutation in human mitochondrial DNA implicated in aminoglycoside-induced ototoxicity.
    Scrimshaw BJ, Faed JM, Tate WP, Yun K.
    J Hum Genet; 1999 Jul; 44(6):388-90. PubMed ID: 10570910
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  • 49. [Mitochondrial DNA A1555G mutation of seven families with nonsyndromic hearing loss].
    Ou QS, Cheng ZJ, Yang B, Jiang L, Chen J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Oct; 26(5):550-4. PubMed ID: 19806580
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  • 50. Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene.
    Mkaouar-Rebai E, Fendri-Kriaa N, Louhichi N, Tlili A, Triki C, Ghorbel A, Masmoudi S, Fakhfakh F.
    Biosci Rep; 2010 Dec; 30(6):405-11. PubMed ID: 20055758
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  • 54. Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.
    Nahili H, Charif M, Boulouiz R, Bounaceur S, Benrahma H, Abidi O, Chafik A, Rouba H, Kandil M, Barakat A.
    Int J Pediatr Otorhinolaryngol; 2010 Sep; 74(9):1071-4. PubMed ID: 20637512
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  • 55. 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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  • 58. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Goto Y, Usami S.
    Ann Otol Rhinol Laryngol; 2005 Feb; 114(2):153-60. PubMed ID: 15757197
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  • 59. Mitochondrial 12S ribosomal RNA A1555G mutation associated with cardiomyopathy and hearing loss following high-dose chemotherapy and repeated aminoglycoside exposure.
    Skou AS, Tranebjærg L, Jensen T, Hasle H.
    J Pediatr; 2014 Feb; 164(2):413-5. PubMed ID: 24252789
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  • 60. [Mutation analysis of 12S rRNA and tRNA-Ser(UCN) genes in a large Chinese family with maternally inherited nonsyndromic hearing loss by intermarriage].
    Shu AL, Ji BH, Qin W, Feng GY, Nie YZ, Liu T, He L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):303-5. PubMed ID: 16767669
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