Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

Annals of Neurology

Volumn 39, Issue 6, 1996, Pages 767-778

  Parchi, Piero ^a   Castellani, Rudolph ^a   Capellari, Sabina ^a   Ghetti, Bernardino ^b   Young, Katherine ^b   Chen, Shu G ^a   Farlow, Martin ^b   Dickson, Dennis W ^c   Sima, Anders A F ^d   Trojanowski, John Q ^e   Petersen, Robert B ^a   Gambetti, Pierluigi ^a  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b INDIANA UNIVERSITY   (United States)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CODON; CREUTZFELDT JAKOB DISEASE; GENE SEQUENCE; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; MOLECULAR GENETICS; PHENOTYPE; PRION; PRIORITY JOURNAL;

ADULT; AGED; ASTROCYTES; BLOTTING, WESTERN; BRAIN; CODON; CREUTZFELDT-JAKOB SYNDROME; CULTURE TECHNIQUES; ENDOPEPTIDASE K; FEMALE; GENOTYPE; GLYCOSYLATION; HOMOZYGOTE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; METHIONINE; MIDDLE AGED; PHENOTYPE; PRIONS; SERINE ENDOPEPTIDASES;

EID: 8944259890     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410390613     Document Type: Article

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