Panencephalitic Creutzfeldt-Jakob disease in a chinese family unusual presentation with PrP codon 210 mutation and identification by PCR-SSCP

Journal of the Neurological Sciences

Volumn 143, Issue 1-2, 1996, Pages 176-180

  Shyu, Woei Cherng ^a   Hsu, Yaw Don ^a   Kao, Ming Ching ^a   Tsao, Wen Long ^a  

^a TRI SERVICE GENERAL HOSPITAL   (Taiwan)

Author keywords

Codon 210 mutation; Creutzfeldt Jakob disease; MPS (1H); MRI; PCR SSCP; White matter degeneration

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CREUTZFELDT JAKOB DISEASE; FAMILIAL DISEASE; FEMALE; HUMAN; MUTATION; NERVE DEGENERATION; PRIORITY JOURNAL;

CHINA; CREUTZFELDT-JAKOB SYNDROME; FAMILY HEALTH; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; PEDIGREE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PRIONS; SEQUENCE ANALYSIS, DNA;

EID: 0030297073     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(96)00198-0     Document Type: Article

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