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Brain and Nerve
Volumn 49, Issue 5, 1997, Pages 460-464
Familial Creutzfeldt Jakob disease with the heterozygous point mutation at codon 200 of the prion protein gene (Glu → Lys): Report of CJD200 brothers of Yamanashi Prefecture origin
Author keywords

codon 200; Creutzfeldt Jakob disease; familial; prion protein gene
Indexed keywords

GLUTAMIC ACID; LYSINE; PRION PROTEIN;
EID: 0030968834     PISSN: 00068969     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)
References (13)
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    • Akai J, Ishihara O, Higuchi S : Creutzfeldt-Jakob disease in Japan : An epidemiological study done in a select prefecture between 1976 and 1986. Neuroepidemiology 8 : 32-37, 1989
    • (1989) Neuroepidemiology , vol.8 , pp. 32-37
    • Akai, J.1    Ishihara, O.2    Higuchi, S.3
  • 3
    • 0026662717 scopus 로고
    • Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy
    • Bertoni JM, Brown P, Goldfarb LG, Rubenstein R, Gajdusek DC : Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy. JAMA 268 : 2413-2415, 1992
    • (1992) JAMA , vol.268 , pp. 2413-2415
    • Bertoni, J.M.1    Brown, P.2    Goldfarb, L.G.3    Rubenstein, R.4    Gajdusek, D.C.5
  • 4
    • 0027443351 scopus 로고
    • Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patient with the PRNP codon 200 mutation
    • Chapman J, Brown P, Goldfarb LG, Arlazoroff A, Gajdusek DC, Korczyn AD: Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patient with the PRNP codon 200 mutation. J Neurol Neurosurg Psychiatry 56 : 1109 -1112, 1993
    • (1993) J Neurol Neurosurg Psychiatry , vol.56 , pp. 1109-1112
    • Chapman, J.1    Brown, P.2    Goldfarb, L.G.3    Arlazoroff, A.4    Gajdusek, D.C.5    Korczyn, A.D.6
  • 5
    • 8244236201 scopus 로고    scopus 로고
    • Japanese source
  • 6
    • 0024992359 scopus 로고
    • Mutation in codon 200 of scrapie amyloid precursor gene linked to Creatzfeldt-Jakob disease in Sephardic Jews of Libyan and non -Libyan origin
    • Goldfarb LG, Korczyn AD, Brown P, Chapman J, Gajdusek DC : Mutation in codon 200 of scrapie amyloid precursor gene linked to Creatzfeldt-Jakob disease in Sephardic Jews of Libyan and non -Libyan origin. Lancet 336 : 639-640, 1990
    • (1990) Lancet , vol.336 , pp. 639-640
    • Goldfarb, L.G.1    Korczyn, A.D.2    Brown, P.3    Chapman, J.4    Gajdusek, D.C.5
  • 8
    • 0025641602 scopus 로고
    • Inherited human prion disease
    • Cleveland
    • Hsiao K, Prusiner SB : Inherited human prion disease. Neurology (Cleveland) 40 : 1820-1827, 1990
    • (1990) Neurology , vol.40 , pp. 1820-1827
    • Hsiao, K.1    Prusiner, S.B.2
  • 9
    • 0028206519 scopus 로고
    • Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene
    • Cleveland
    • Inoue I, Kitamoto T, Doh-ura, K, Shii H, Goto I, Tateishi J : Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene. Neurology (Cleveland) 44 : 299 -301, 1994
    • (1994) Neurology , vol.44 , pp. 299-301
    • Inoue, I.1    Kitamoto, T.2    Doh-ura, K.3    Shii, H.4    Goto, I.5    Tateishi, J.6
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  • 12
    • 8244259647 scopus 로고    scopus 로고
    • Japanese source
  • 13
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    • Familial Creutzfeldt-Jakob disease in Japan : Three cases in a family with white matter involvement
    • Yamamoto T, Nagashima K, Tsubaki T, Oikawa K, Akai J : Familial Creutzfeldt-Jakob disease in Japan : Three cases in a family with white matter involvement. J Neurol Sci 67 : 119-130, 1985
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.