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Volumn 572, Issue , 2005, Pages 3-8

Genetic factors modifying clinical expression of autosomal dominant RP

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; EYE PROTEINS; FEMALE; GENE EXPRESSION REGULATION; GENES, DOMINANT; GENETIC LINKAGE; HUMANS; INFANT; INFANT, NEWBORN; LINKAGE (GENETICS); MALE; MIDDLE AGED; MODELS, GENETIC; POLYMORPHISM, GENETIC; RETINITIS PIGMENTOSA;

EID: 33747435512     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: None     Document Type: Conference Paper
Times cited : (9)

References (27)
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    • Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees
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    • (1999) Am. J. Hum. Genet. , vol.64 , pp. 839-851
    • Daw, E.W.1    Heath, S.C.2    Wijsman, E.M.3
  • 10
    • 0028606982 scopus 로고
    • Human genetics. Silence speaks in spectrin
    • Gratzer, W., 1994, Human genetics. Silence speaks in spectrin. Nat. 372:620-621.
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    • Gratzer, W.1
  • 13
    • 0030833349 scopus 로고    scopus 로고
    • Markov chain Monte Carlo segregation and linkage analysis for oligogenic models
    • Heath, S. C., 1997, Markov chain Monte Carlo segregation and linkage analysis for oligogenic models, Am. J. Hum. Genet. 61:748-760.
    • (1997) Am. J. Hum. Genet. , vol.61 , pp. 748-760
    • Heath, S.C.1
  • 19
    • 3242749615 scopus 로고    scopus 로고
    • The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein
    • Liu, Q., Zuo, J., Pierce, E. A., 2004, The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein, J. Neurosci. 24:6427-6436.
    • (2004) J. Neurosci. , vol.24 , pp. 6427-6436
    • Liu, Q.1    Zuo, J.2    Pierce, E.A.3
  • 20
    • 0030731399 scopus 로고    scopus 로고
    • Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele
    • McGee, T. L., Devoto, M., Ott, J., Berson, E. L., Dryja, T. P., 1997, Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele, Am. J. Hum. Genet. 61:1059-1066.
    • (1997) Am. J. Hum. Genet. , vol.61 , pp. 1059-1066
    • McGee, T.L.1    Devoto, M.2    Ott, J.3    Berson, E.L.4    Dryja, T.P.5
  • 21
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    • Modifier genes and protective alleles in humans and mice
    • Nadeau J., 2003, Modifier genes and protective alleles in humans and mice, Curr. Opin. Genet. Dev. 3:290-295.
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    • Nadeau, J.1
  • 22
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    • Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa
    • Pierce, E. A., Quinn, T., Meehan, T., McGee, T. L., Berson, E. L., Dryja, T. P., 1999, Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa, Nat. Genet. 22:48-254.
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    • Pierce, E.A.1    Quinn, T.2    Meehan, T.3    McGee, T.L.4    Berson, E.L.5    Dryja, T.P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.