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Volumn 59, Issue 2 A, 2001, Pages 161-164

Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17

Author keywords

Creutzfeldt jakob disease; Frontotemporal dementia; Parkinsonism; Prion disease; Prion protein mutation

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 17; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DIFFERENTIAL DIAGNOSIS; FEMALE; GENETIC LINKAGE; GENETICS; HUMAN; MALE; MIDDLE AGED; PARKINSONISM; PEDIGREE;

EID: 0035377470     PISSN: 0004282X     EISSN: None     Source Type: Journal    
DOI: 10.1590/S0004-282X2001000200001     Document Type: Article
Times cited : (30)

References (10)
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    • Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene
    • Goldfarb LG, Brown P, Mc Combie WR, et al. Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. Proc Natl Acad Sci USA 1991;88:10296-10930.
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  • 10
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    • Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene
    • Laplanche JL, El Hachimi KH, Durieux I, et al. Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene. Brain 1999;122:2375-2386.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.