Creutzfeldt-Jakob disease in a young person with valine homozygosity at codon 129: Sporadic or variant? [4]

Journal of Neurology Neurosurgery and Psychiatry

Volumn 70, Issue 1, 2001, Pages 134-135

  Hillier, C E M ^a   Llewelyn, J G ^a   Neal, J W ^a   Ironside, J W ^a  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN; VALINE;

ADULT; ANXIETY; AUTOPSY; BRAIN ATROPHY; BRAIN SPONGIOSIS; CASE REPORT; CLINICAL FEATURE; CODON; CREUTZFELDT JAKOB DISEASE; DETERIORATION; DIAGNOSTIC APPROACH ROUTE; DYSPHASIA; GENOTYPE; HOMOZYGOTE; HUMAN; LETTER; MALE; NEUROPATHOLOGY; PRIORITY JOURNAL; SYMPTOM;

ADULT; CODON; CREUTZFELDT-JAKOB SYNDROME; HOMOZYGOTE; HUMANS; MALE; VALINE;

EID: 0035136494     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.70.1.134     Document Type: Letter

References (5)

1. Codon 129 genotype and new variant CJD
2. The same prion protein strain causes vCJD and BSE
3. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
4. Molecular analysis of prion strain variation and the aetiology of new variant CJD