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Journal Abstract Search

113 related items for PubMed ID: 18229583

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  • 6. GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.
    Guo YF, Liu XW, Guan J, Han MK, Wang DY, Zhao YL, Rao SQ, Wang QJ.
    Acta Otolaryngol; 2008 Mar; 128(3):297-303. PubMed ID: 18274916
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  • 7. Audiological and genetic features of the mtDNA mutations.
    Liu XZ, Angeli S, Ouyang XM, Liu W, Ke XM, Liu YH, Liu SX, Du LL, Deng XW, Yuan H, Yan D.
    Acta Otolaryngol; 2008 Jul; 128(7):732-8. PubMed ID: 18568513
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  • 9. [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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  • 10. [Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].
    Liu X, Dai P, Huang DL, Yuan HJ, Li WM, Cao JY, Yu F, Zhang RN, Lin HY, Zhu XH, He Y, Yu YJ, Yao K.
    Zhonghua Yi Xue Za Zhi; 2006 May 23; 86(19):1318-22. PubMed ID: 16796900
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  • 12. [Mitochondrial 12S rRNA gene A827G in two pedigrees with nonsyndromic deafness].
    Chen ZB, Cao X, Xing GQ, Tian HQ, Zhou AD, Wei QU, Bu XK.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug 23; 23(4):415-8. PubMed ID: 16883529
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  • 13. Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation.
    Young WY, Zhao L, Qian Y, Wang Q, Li N, Greinwald JH, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1244-51. PubMed ID: 15708009
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  • 14. Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S.
    Laryngoscope; 2004 Jun 25; 114(6):1085-91. PubMed ID: 15179218
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  • 17. Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.
    Montazer Zohour M, Tabatabaiefar MA, Dehkordi FA, Farrokhi E, Akbari MT, Chaleshtori MH.
    Genet Test Mol Biomarkers; 2012 Apr 25; 16(4):271-8. PubMed ID: 22077646
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  • 18. Molecular epidemiological analysis of mitochondrial DNA12SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sensorineural hearing loss in China.
    Ji YB, Han DY, Lan L, Wang DY, Zong L, Zhao FF, Liu Q, Benedict-Alderfer C, Zheng QY, Wang QJ.
    Acta Otolaryngol; 2011 Feb 25; 131(2):124-9. PubMed ID: 21162657
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