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Journal Abstract Search

210 related items for PubMed ID: 9002678

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  • 3. Defective myosin VIIA gene responsible for Usher syndrome type 1B.
    Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD.
    Nature; 1995 Mar 02; 374(6517):60-1. PubMed ID: 7870171
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  • 6. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.
    Kumar A, Babu M, Kimberling WJ, Venkatesh CP.
    Mol Vis; 2004 Nov 24; 10():910-6. PubMed ID: 15592175
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  • 9. Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.
    Nájera C, Beneyto M, Blanca J, Aller E, Fontcuberta A, Millán JM, Ayuso C.
    Hum Mutat; 2002 Jul 24; 20(1):76-7. PubMed ID: 12112664
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  • 10. Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome.
    Espinós C, Millán JM, Sánchez F, Beneyto M, Nájera C.
    Hum Genet; 1998 Jun 24; 102(6):691-4. PubMed ID: 9703432
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  • 11. Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis.
    Ben-Rebeh I, Grati M, Bonnet C, Bouassida W, Hadjamor I, Ayadi H, Ghorbel A, Petit C, Masmoudi S.
    Mol Vis; 2016 Jun 24; 22():827-35. PubMed ID: 27440999
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  • 13. Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I.
    Bharadwaj AK, Kasztejna JP, Huq S, Berson EL, Dryja TP.
    Exp Eye Res; 2000 Aug 24; 71(2):173-81. PubMed ID: 10930322
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  • 14. Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients.
    Weston MD, Kelley PM, Overbeck LD, Wagenaar M, Orten DJ, Hasson T, Chen ZY, Corey D, Mooseker M, Sumegi J, Cremers C, Moller C, Jacobson SG, Gorin MB, Kimberling WJ.
    Am J Hum Genet; 1996 Nov 24; 59(5):1074-83. PubMed ID: 8900236
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  • 15. Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans.
    Orten DJ, Weston MD, Kelley PM, Cremers CW, Wagenaar M, Jacobson SG, Kimberling WJ.
    Hum Mutat; 2000 Jan 24; 15(1):114-5. PubMed ID: 10612833
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  • 17. Identification of three novel mutations in the MYO7A gene.
    Cuevas JM, Espinós C, Millán JM, Sánchez F, Trujillo MJ, Ayuso C, Beneyto M, Nájera C.
    Hum Mutat; 1999 Aug 19; 14(2):181. PubMed ID: 10447383
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  • 20. Molecular genetics of Usher syndrome.
    Eudy JD, Sumegi J.
    Cell Mol Life Sci; 1999 Oct 15; 56(3-4):258-67. PubMed ID: 11212353
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