Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 14, 1998, Pages 8322-8327

  Parchi, Piero ^a   Chen, Shu G ^a   Brown, Paul ^b   Zou, Wenquan ^a   Capellari, Sabina ^a   Budka, Herbert ^c,d   Hainfellner, Johannes ^c,d   Reyes, Patricio F ^f,g   Golden, Gregory T ^f,g   Hauw, Jean J ^e   Gajdusek, D Carleton ^b   Gambetti, Pierluigi ^a  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^c MEDICAL UNIVERSITY OF VIENNA   (Austria)

^d MEDICAL UNIVERSITY OF VIENNA   (Austria)

^e PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^f THOMAS JEFFERSON UNIVERSITY   (United States)

^g VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; PRION PROTEIN; PROTEINASE;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CODON; FEMALE; GENE; GENE MUTATION; GERSTMANN STRAUSSLER SCHEINKER SYNDROME; HAPLOTYPE; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IMMUNOBLOTTING; MALE; MASS SPECTROMETRY; PHENOTYPE; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL;

ADULT; AGED; FEMALE; GENETIC MARKERS; GERSTMANN-STRAUSSLER-SCHEINKER DISEASE; HUMANS; MALE; MIDDLE AGED; MUTATION; PEPTIDE FRAGMENTS; PRIONS;

EID: 0032493453     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.14.8322     Document Type: Article

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