Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: Relationship with sporadic CJD

American Journal of Pathology

Volumn 167, Issue 6, 2005, Pages 1729-1738

  Pastore, Manuela ^a   Chin, Steven S ^c   Bell, Karen L ^d   Dong, Zhiqian ^a,b   Yang, Qiwei ^a   Yang, Lizhu ^a,b   Yuan, Jue ^a,b   Chen, Shu G ^a,b   Gambetti, Pierluigi ^a,b   Zou, Wen Quan ^a,b  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b National Prion Disease Pathology Surveillance Center   (United States)

^c UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

^d Columbia University College of Physicians and Surgeons ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ISOPROTEIN; METHIONINE; PRION PROTEIN; VALINE;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CODON; CREUTZFELDT JAKOB DISEASE; FEMALE; GENE; GENE LOCATION; GENE MUTATION; GENOTYPE; HOMOZYGOSITY; HUMAN; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PRNP GENE;

EID: 28244491680     PISSN: 00029440     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9440(10)61254-0     Document Type: Article

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