IDENTIFICATION OF A PRNP GENE MUTATION IN JAKOBS ORIGINAL CREUTZFELDT-JAKOB-DISEASE FAMILY

被引：18

作者：

BROWN, P

CERVENAKOVA, L

BOELLAARD, JW

STAVROU, D

GOLDFARB, LG

GAJDUSEK, DC

机构：

[1] UNIV HAMBURG,KRANKENHAUS EPPENDORF,INST PATHOL,W-2000 HAMBURG,GERMANY

[2] UNIV TUBINGEN,INST HIRNFORSCH,TUBINGEN,GERMANY

来源：

LANCET | 1994年 / 344卷 / 8915期

关键词：

D O I：

10.1016/S0140-6736(94)91318-8

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：130 / 131

页数：2

共 5 条

[1] PHENOTYPIC CHARACTERISTICS OF FAMILIAL CREUTZFELDT-JAKOB DISEASE ASSOCIATED WITH THE CODON-178ASN PRNP MUTATION [J].

BROWN, P ;

GOLDFARB, LG ;

KOVANEN, J ;

HALTIA, M ;

CATHALA, F ;

SULIMA, M ;

GIBBS, CJ ;

GAJDUSEK, DC .

ANNALS OF NEUROLOGY, 1992, 31 (03) :282-285

[2] NEW MUTATION IN SCRAPIE AMYLOID PRECURSOR GENE (AT CODON-178) IN FINNISH CREUTZFELDT-JAKOB KINDRED [J].

GOLDFARB, LG ;

HALTIA, M ;

BROWN, P ;

NIETO, A ;

KOVANEN, J ;

MCCOMBIE, WR ;

TRAPP, S ;

GAJDUSEK, DC .

LANCET, 1991, 337 (8738) :425-425

[3]

JACOB H, 1950, Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr, V184, P653, DOI 10.1007/BF00344941

[4]

JAKOB A, 1923, MONOGR PSYCHIAT BERL, V37, P215

[5] Two peculiar diseases of the central nervous system after a type of spastic pseudosclerosis (Jakob) [J].

Kirschbaum, W .

ZEITSCHRIFT FUR DIE GESAMTE NEUROLOGIE UND PSYCHIATRIE, 1924, 92 :175-220

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