Basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

Neurology

Volumn 52, Issue 6, 1999, Pages 1244-1249

  Tranchant, C ^b   Geranton, L ^c   Guiraud Chaumeil, C ^c   Mohr, M ^a   Warter, J M ^c  

^a Institut de Pathologie Strasbourg   (France)

^b UNIVERSITY HOSPITAL OF STRASBOURG   (France)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE; PRION PROTEIN;

ADULT; AGED; ARTICLE; CEREBELLAR ATAXIA; CLINICAL ARTICLE; CODON; CREUTZFELDT JAKOB DISEASE; DEMENTIA; FEMALE; GENETIC VARIABILITY; HUMAN; HUMAN TISSUE; MALE; MYOCLONUS; PHENOTYPE; PRION DISEASE; PRIORITY JOURNAL;

EID: 0032919450     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.52.6.1244     Document Type: Article

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