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374 related items for PubMed ID: 9590435

  • 1. Coding sequence and exon/intron organization of the canine CLN3 (Batten disease) gene and its exclusion as the locus for ceroid-lipofuscinosis in English setter dogs.
    Shibuya H, Liu PC, Katz ML, Siakotos AN, Nonneman DJ, Johnson GS.
    J Neurosci Res; 1998 May 01; 52(3):268-75. PubMed ID: 9590435
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  • 5. Profound infantile neuroretinal dysfunction in a heterozygote for the CLN3 genetic defect.
    de los Reyes E, Dyken PR, Phillips P, Brodsky M, Bates S, Glasier C, Mrak RE.
    J Child Neurol; 2004 Jan 01; 19(1):42-6. PubMed ID: 15032383
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  • 8. A novel c.1135_1138delCTGT mutation in CLN3 leads to juvenile neuronal ceroid lipofuscinosis.
    Drack AV, Miller JN, Pearce DA.
    J Child Neurol; 2013 Sep 01; 28(9):1112-6. PubMed ID: 23877479
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  • 14. Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth.
    Cotman SL, Vrbanac V, Lebel LA, Lee RL, Johnson KA, Donahue LR, Teed AM, Antonellis K, Bronson RT, Lerner TJ, MacDonald ME.
    Hum Mol Genet; 2002 Oct 15; 11(22):2709-21. PubMed ID: 12374761
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  • 16. Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse models.
    Chan CH, Mitchison HM, Pearce DA.
    Hum Mol Genet; 2008 Nov 01; 17(21):3332-9. PubMed ID: 18678598
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