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Journal Abstract Search

131 related items for PubMed ID: 12584878

  • 21. 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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  • 22. Study of mitochondrial DNA A1555G and C1494T mutations in a large cohort of women individuals.
    Wang L, Wang X, Cai X, Qiang R.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2019 Mar; 30(2):222-225. PubMed ID: 29790807
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  • 29. 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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  • 30. Pharmacogenetic screening of A1555G and C1494T mitochondrial mutations and the use of ototoxic drugs among Jordanians.
    Yehya A, Al-Trad B, Bani-Hmoud M, Rababa'h AM.
    Eur Rev Med Pharmacol Sci; 2021 Sep; 25(18):5684-5689. PubMed ID: 34604960
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  • 33. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation.
    Tono T, Ushisako Y, Kiyomizu K, Usami S, Abe S, Shinkawa H, Komune S.
    Am J Otol; 1998 Nov; 19(6):754-7. PubMed ID: 9831149
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  • 34. [Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycoside treatment].
    Morales Angulo C, Gallo-Terán J, Señaris B, Fontalva A, González-Aguado R, Fernández-Luna JL.
    Acta Otorrinolaringol Esp; 2011 Nov; 62(2):83-6. PubMed ID: 21129708
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  • 35. 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; 28(3):332-42. PubMed ID: 17485982
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  • 38. The A1555G mtDNA mutation in Danish hearing-impaired patients: frequency and clinical signs.
    ØStergaard E, Montserrat-Sentis B, Grønskov K, Brøndum-Nielsen K.
    Clin Genet; 2002 Oct; 62(4):303-5. PubMed ID: 12372057
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  • 39. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
    Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ.
    Eur J Hum Genet; 1998 Oct; 6(6):563-9. PubMed ID: 9887373
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