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Journal Abstract Search

332 related items for PubMed ID: 18340555

  • 1. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
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  • 3. Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNASerUCN gene in a Japanese family.
    Li R, Ishikawa K, Deng JH, Heman-Ackah S, Tamagawa Y, Yang L, Bai Y, Ichimura K, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 04; 328(1):32-7. PubMed ID: 15670746
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  • 4. Familial auditory neuropathy.
    Wang Q, Gu R, Han D, Yang W.
    Laryngoscope; 2003 Sep 04; 113(9):1623-9. PubMed ID: 12972945
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  • 7. 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 04; 114(2):153-60. PubMed ID: 15757197
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  • 8. 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 04; 10(12):851-6. PubMed ID: 12461693
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  • 9. Audiologic findings in patients with a point mutation at nucleotide 3,243 of mitochondrial DNA.
    Tamagawa Y, Kitamura K, Hagiwara H, Ishida T, Nishizawa M, Saito T, Iwamoto Y.
    Ann Otol Rhinol Laryngol; 1997 Apr 04; 106(4):338-42. PubMed ID: 9109727
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  • 12. Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF).
    Rodríguez-Ballesteros M, del Castillo FJ, Martín Y, Moreno-Pelayo MA, Morera C, Prieto F, Marco J, Morant A, Gallo-Terán J, Morales-Angulo C, Navas C, Trinidad G, Tapia MC, Moreno F, del Castillo I.
    Hum Mutat; 2003 Dec 04; 22(6):451-6. PubMed ID: 14635104
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  • 16. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.
    Tang X, Li R, Zheng J, Cai Q, Zhang T, Gong S, Zheng W, He X, Zhu Y, Xue L, Yang A, Yang L, Lu J, Guan MX.
    Mol Genet Metab; 2010 May 04; 100(1):57-64. PubMed ID: 20153673
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  • 18. Auditory findings in patients with maternally inherited diabetes and deafness harboring a point mutation in the mitochondrial transfer RNA(Leu) (UUR) gene.
    Yamasoba T, Oka Y, Tsukuda K, Nakamura M, Kaga K.
    Laryngoscope; 1996 Jan 04; 106(1 Pt 1):49-53. PubMed ID: 8544627
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  • 20. Audiologic aspects of the search for DFNA20: a gene causing late-onset, progressive, sensorineural hearing loss.
    Elfenbein JL, Fisher RA, Wei S, Morell RJ, Stewart C, Friedman TB, Friderici K.
    Ear Hear; 2001 Aug 04; 22(4):279-88. PubMed ID: 11527035
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