Mutation of the prion protein gene at codon 208 in familial Creutzfeldt- Jakob disease

Neurology

Volumn 47, Issue 5, 1996, Pages 1305-1312

  Mastrianni, J A ^a   Iannicola, C ^b   Myers, R M ^b   DeArmond, S ^a   Prusiner, S B ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b STANFORD UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; ARGININE; GENE PRODUCT; GUANINE; HISTIDINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CODON; CREUTZFELDT JAKOB DISEASE; DENATURING GRADIENT GEL ELECTROPHORESIS; DNA SEQUENCE; GENE MUTATION; GENETIC LINKAGE; HUMAN; HUMAN TISSUE; MALE; OPEN READING FRAME; PRION DISEASE; PRIORITY JOURNAL;

EID: 0029905230     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.47.5.1305     Document Type: Article

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