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Volumn 24, Issue 1-2, 2005, Pages 103-109

Familial prion diseases in the basque country (Spain)

Author keywords

Creutzfeldt jakob disease; D178n mutation; E200k mutation; Fatal familial insomnia; Prion

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GENEALOGY; GENETICS; HUMAN; HUMAN TISSUE; MALE; PRION DISEASE; SPAIN;

EID: 10844250074     PISSN: 02515350     EISSN: None     Source Type: Journal    
DOI: 10.1159/000081057     Document Type: Article
Times cited : (8)

References (22)
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  • 6
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    • Budka, H.1    Aguzzi, A.2    Brown, P.3    Brucher, J.M.4    Bugiani, O.5    Colling, J.6    Diringer, H.7
  • 9
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    • Mitrova, E.1
  • 10
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  • 16
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    • Identification in Israel of two Jewish Creutzfeldt-Jakob disease patients with a 178 mutation at their PrP gene
    • Rosenmann H, Vardi J, Finkelstein Y, Chapman J, Gabizon R: Identification in Israel of two Jewish Creutzfeldt-Jakob disease patients with a 178 mutation at their PrP gene. Acta Neurol Scand 1998;97:184-187.
    • (1998) Acta Neurol Scand , vol.97 , pp. 184-187
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.