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Journal Abstract Search

164 related items for PubMed ID: 10532406

  • 1. Electrophysiological findings in dominant optic atrophy (DOA) linking to the OPA1 locus on chromosome 3q 28-qter.
    Holder GE, Votruba M, Carter AC, Bhattacharya SS, Fitzke FW, Moore AT.
    Doc Ophthalmol; ; 95(3-4):217-28. PubMed ID: 10532406
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  • 4. Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy.
    Meyer E, Michaelides M, Tee LJ, Robson AG, Rahman F, Pasha S, Luxon LM, Moore AT, Maher ER.
    Mol Vis; 2010 Apr 13; 16():650-64. PubMed ID: 20405026
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  • 7. Pattern electroretinogram (PERG) and pattern visual evoked potential (PVEP) in the early stages of Alzheimer's disease.
    Krasodomska K, Lubiński W, Potemkowski A, Honczarenko K.
    Doc Ophthalmol; 2010 Oct 13; 121(2):111-21. PubMed ID: 20549299
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  • 8. Electrophysiology and colour perimetry in dominant infantile optic atrophy.
    Berninger TA, Jaeger W, Krastel H.
    Br J Ophthalmol; 1991 Jan 13; 75(1):49-52. PubMed ID: 1991088
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  • 9. Dominant optic atrophy, Kjer type. Linkage analysis and clinical features in a large British pedigree.
    Johnston RL, Burdon MA, Spalton DJ, Bryant SP, Behnam JT, Seller MJ.
    Arch Ophthalmol; 1997 Jan 13; 115(1):100-3. PubMed ID: 9006433
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  • 10. Demonstration of a founder effect and fine mapping of dominant optic atrophy locus on 3q28-qter by linkage disequilibrium method: a study of 38 British Isles pedigrees.
    Votruba M, Moore AT, Bhattacharya SS.
    Hum Genet; 1998 Jan 13; 102(1):79-86. PubMed ID: 9490303
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  • 11. Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3.
    Kerrison JB, Arnould VJ, Ferraz Sallum JM, Vagefi MR, Barmada MM, Li Y, Zhu D, Maumenee IH.
    Arch Ophthalmol; 1999 Jun 13; 117(6):805-10. PubMed ID: 10369594
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  • 15. Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.
    Votruba M, Moore AT, Bhattacharya SS.
    J Med Genet; 1998 Oct 13; 35(10):793-800. PubMed ID: 9783700
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  • 19. Dominant optic atrophy. Refining the clinical diagnostic criteria in light of genetic linkage studies.
    Johnston RL, Seller MJ, Behnam JT, Burdon MA, Spalton DJ.
    Ophthalmology; 1999 Jan 13; 106(1):123-8. PubMed ID: 9917792
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  • 20. Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q.
    Votruba M, Moore AT, Bhattacharya SS.
    J Med Genet; 1997 Feb 13; 34(2):117-21. PubMed ID: 9039986
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