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Volumn 44, Issue 3, 1999, Pages 211-212

A case-report on a carrier of the PRA-causing mutation in Irish Setters in Germany;Fallbeschreibung eines PRA-Gen-Trägers bei Irish Settern in Deutschland

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Indexed keywords


EID: 0347180275     PISSN: 00232076     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (8)
  • 1
    • 0024852932 scopus 로고
    • Non-allelism of three genes (rcd1, rcd2 and erd) for early-onset hereditary retinal degeneration
    • ACLAND, G., R. T. FLETCHER, S. GENTLEMAN, G. CHADER und G. D. AGUIRRE (1989): Non-allelism of three genes (rcd1, rcd2 and erd) for early-onset hereditary retinal degeneration. Exp. Eye Res. 49, 983-998.
    • (1989) Exp. Eye Res. , vol.49 , pp. 983-998
    • Acland, G.1    Fletcher, R.T.2    Gentleman, S.3    Chader, G.4    Aguirre, G.D.5
  • 2
    • 84980123035 scopus 로고
    • Canine retinopathies: III: The other breeds
    • BARNETT, K. C. (1965): Canine retinopathies: III: The other breeds. J. Small Anim. Pract. 6, 185-196.
    • (1965) J. Small Anim. Pract. , vol.6 , pp. 185-196
    • Barnett, K.C.1
  • 3
    • 0027521606 scopus 로고
    • Confirmation of the rod cGMP phosphodiesterase β-subunit (PDEβ) nonsense mutation in affected rcd-1 Irish setters in the UK and development of a diagnostic test
    • CLEMENTS, P. J. M., C. Y. GREGORY, S. M. PETERSEN-JONES, D. R. SARGAN und S. S. BHATTACHARYA (1993): Confirmation of the rod cGMP phosphodiesterase β-subunit (PDEβ) nonsense mutation in affected rcd-1 Irish setters in the UK and development of a diagnostic test. Curr. Eye Res. 12, 861-866.
    • (1993) Curr. Eye Res. , vol.12 , pp. 861-866
    • Clements, P.J.M.1    Gregory, C.Y.2    Petersen-Jones, S.M.3    Sargan, D.R.4    Bhattacharya, S.S.5
  • 5
    • 0027946102 scopus 로고
    • Cosegregation of Codon 807 Mutation of the Canine Rod cGMP Phosphodiesterase β-Gene and rcd1
    • RAY, K., V. J. BALDWIN, G. M. ACLAND, S. H. BLANTON und G. D. AGUIRRE (1994): Cosegregation of Codon 807 Mutation of the Canine Rod cGMP Phosphodiesterase β-Gene and rcd1. Invest. Ophthalmol. & Vis. Sci. 35, 4291-4299.
    • (1994) Invest. Ophthalmol. & Vis. Sci. , vol.35 , pp. 4291-4299
    • Ray, K.1    Baldwin, V.J.2    Acland, G.M.3    Blanton, S.H.4    Aguirre, G.D.5
  • 6
    • 84980123035 scopus 로고
    • Canine retinopathies: III: The other breeds
    • zitiert in BARNETT, K. C. (1965)
    • RASBRIDGE, W. J. (1965); zitiert in BARNETT, K. C. (1965): Canine retinopathies: III: The other breeds. J. Small Anim. Pract. 6, 185-196.
    • (1965) J. Small Anim. Pract. , vol.6 , pp. 185-196
    • Rasbridge, W.J.1
  • 7
    • 84980123035 scopus 로고
    • Canine retinopathies: III: The other breeds
    • zitiert in BARNETT, K. C. (1965)
    • WOOLRIDGE, W. R., und J. A. F. ROBERTS (1965); zitiert in BARNETT, K. C. (1965): Canine retinopathies: III: The other breeds. J. Small Anim. Pract. 6, 185-196.
    • (1965) J. Small Anim. Pract. , vol.6 , pp. 185-196
    • Woolridge, W.R.1    Roberts, J.A.F.2
  • 8
    • 0029337315 scopus 로고
    • Incidence of the gene mutation causal for rodcone dysplasia type 1 in Irish setters in the UK
    • PETERSENJONES, S. M., P. J. M. CLEMENTS, K. C. BARNETT und D. R. SARGAN (1995): Incidence of the gene mutation causal for rodcone dysplasia type 1 in Irish setters in the UK. J. Small Anim. Prac. 36, 310-314.
    • (1995) J. Small Anim. Prac. , vol.36 , pp. 310-314
    • Petersenjones, S.M.1    Clements, P.J.M.2    Barnett, K.C.3    Sargan, D.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.