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Journal Abstract Search

201 related items for PubMed ID: 11978760

  • 21. [Analysis of rhodopsin and peripherin/RDS genes in Chinese patients with retinitis pigmentosa].
    Zhang F, Zhang Q, Shen H, Li S, Xiao X.
    Yan Ke Xue Bao; 1998 Dec; 14(4):210-4. PubMed ID: 12579739
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  • 25. A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa.
    Farrar GJ, Kenna P, Jordan SA, Kumar-Singh R, Humphries MM, Sharp EM, Sheils DM, Humphries P.
    Nature; 1991 Dec 12; 354(6353):478-80. PubMed ID: 1749427
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  • 26. Two novel missense mutations in the peripherin/RDS gene in two unrelated French patients with autosomal dominant retinitis pigmentosa.
    Souied EH, Rozet JM, Gerber S, Dufier JL, Soubrane G, Coscas G, Munnich A, Kaplan J.
    Eur J Ophthalmol; 1998 Dec 12; 8(2):98-101. PubMed ID: 9673478
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  • 32. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci.
    Kajiwara K, Berson EL, Dryja TP.
    Science; 1994 Jun 10; 264(5165):1604-8. PubMed ID: 8202715
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  • 37. Pattern dystrophy and retinitis pigmentosa caused by a peripherin/RDS mutation.
    Richards SC, Creel DJ.
    Retina; 1995 Jun 10; 15(1):68-72. PubMed ID: 7754251
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