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Journal Abstract Search

356 related items for PubMed ID: 10393062

  • 1. Frequency of mutations in the gene encoding the alpha subunit of rod cGMP-phosphodiesterase in autosomal recessive retinitis pigmentosa.
    Dryja TP, Rucinski DE, Chen SH, Berson EL.
    Invest Ophthalmol Vis Sci; 1999 Jul; 40(8):1859-65. PubMed ID: 10393062
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  • 2. Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase.
    Huang SH, Pittler SJ, Huang X, Oliveira L, Berson EL, Dryja TP.
    Nat Genet; 1995 Dec; 11(4):468-71. PubMed ID: 7493036
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  • 3. cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog.
    Petersen-Jones SM, Entz DD, Sargan DR.
    Invest Ophthalmol Vis Sci; 1999 Jul; 40(8):1637-44. PubMed ID: 10393029
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  • 4. [Identification of 2 allelic mutations of the gene of the phosphodiesterase beta subunit in a Spanish family with recessive autosomic retinitis pigmentosa].
    Baiget M, Calaf M, Valverde D, del Río E, Reig C, Carballo M, Calvo MT, González-Duarte R.
    Med Clin (Barc); 1998 Oct 10; 111(11):420-2. PubMed ID: 9834916
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  • 5. Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerations.
    Gao YQ, Danciger M, Longmuir R, Piriev NI, Zhao DY, Heckenlively JR, Fishman GA, Weleber RG, Jacobson SG, Stone EM, Farber DB.
    Invest Ophthalmol Vis Sci; 1999 Jul 10; 40(8):1818-22. PubMed ID: 10393054
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  • 14. A novel homozygous Ile535Asn mutation in the rod cGMP phosphodiesterase beta-subunit gene in two brothers of a Japanese family with autosomal recessive retinitis pigmentosa.
    Saga M, Mashima Y, Akeo K, Kudoh J, Oguchi Y, Shimizu N.
    Curr Eye Res; 1998 Mar 10; 17(3):332-5. PubMed ID: 9543643
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  • 15. Screening of the PDE6B gene in patients with autosomal dominant retinitis pigmentosa.
    Gao YQ, Danciger M, Zhao DY, Blaney J, Piriev NI, Shih J, Jacobson SG, Heckenlively JH, Farber DB.
    Exp Eye Res; 1996 Feb 10; 62(2):149-54. PubMed ID: 8698075
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  • 18. Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1).
    Berson EL, Grimsby JL, Adams SM, McGee TL, Sweklo E, Pierce EA, Sandberg MA, Dryja TP.
    Invest Ophthalmol Vis Sci; 2001 Sep 10; 42(10):2217-24. PubMed ID: 11527933
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  • 20. Evaluation of cGMP-phosphodiesterase (PDE) subunits for causal association with rod-cone dysplasia 2 (rcd2), a canine model of abnormal retinal cGMP metabolism.
    Wang W, Acland GM, Ray K, Aguirre GD.
    Exp Eye Res; 1999 Oct 10; 69(4):445-53. PubMed ID: 10504278
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