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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

114 related items for PubMed ID: 11332404

  • 41. The COCH gene: a frequent cause of hearing impairment and vestibular dysfunction?
    Fransen E, Van Camp G.
    Br J Audiol; 1999 Oct; 33(5):297-302. PubMed ID: 10890144
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  • 42. Genomic study of a large family with complex neurological phenotype including hearing loss, imbalance and action tremor.
    Bally JF, Zhang M, Dwosh E, Sato C, Rutka J, Lang AE, Rogaeva E.
    Neurobiol Aging; 2022 May; 113():137-142. PubMed ID: 35063306
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  • 43. Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin.
    Grabski R, Szul T, Sasaki T, Timpl R, Mayne R, Hicks B, Sztul E.
    Hum Genet; 2003 Oct; 113(5):406-16. PubMed ID: 12928864
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  • 44. Extralabyrinthine manifestations of DFNA9.
    McCall AA, Linthicum FH, O'Malley JT, Adams JC, Merchant SN, Bassim MK, Gellibolian R, Fayad JN.
    J Assoc Res Otolaryngol; 2011 Apr; 12(2):141-9. PubMed ID: 21052762
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  • 47. Different Phenotypes of the Two Chinese Probands with the Same c.889G>A (p.C162Y) Mutation in COCH Gene Verify Different Mechanisms Underlying Autosomal Dominant Nonsyndromic Deafness 9.
    Wang Q, Fei P, Gu H, Zhang Y, Ke X, Liu Y.
    PLoS One; 2017 Apr; 12(1):e0170011. PubMed ID: 28099493
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  • 54. Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.
    Makishima T, Rodriguez CI, Robertson NG, Morton CC, Stewart CL, Griffith AJ.
    Hum Genet; 2005 Oct; 118(1):29-34. PubMed ID: 16078052
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  • 55. Identification of MYO6 copy number variation associated with cochlear aplasia by targeted sequencing.
    Sun L, Wang X, Hou S, Liang M, Yang J.
    Int J Pediatr Otorhinolaryngol; 2020 Jan; 128():109689. PubMed ID: 31785455
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  • 56. A clone contig of 12q24.3 encompassing the distal hereditary motor neuropathy type II gene.
    Irobi J, Tissir F, De Jonghe P, De Vriendt E, Van Broeckhoven C, Timmerman V, Beuten J.
    Genomics; 2000 Apr 01; 65(1):34-43. PubMed ID: 10777663
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  • 59. Attitudes of Potential Participants Towards Potential Gene Therapy Trials in Autosomal Dominant Progressive Sensorineural Hearing Loss.
    Levie C, Moyaert J, Janssens de Varebeke S, Verdoodt D, Vanderveken OM, Topsakal V, Van Wijk E, de Vrieze E, Pennings R, Van de Berg R, Van Camp G, Ponsaerts P, Van Rompaey V.
    Otol Neurotol; 2021 Mar 01; 42(3):384-389. PubMed ID: 33555744
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  • 60. A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations.
    Pfister M, Thiele H, Van Camp G, Fransen E, Apaydin F, Aydin O, Leistenschneider P, Devoto M, Zenner HP, Blin N, Nürnberg P, Ozkarakas H, Kupka S.
    Cell Physiol Biochem; 2004 Mar 01; 14(4-6):369-76. PubMed ID: 15319541
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