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

被引：16
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
收藏
页码：130 / 131
页数：2
相关论文
共 5 条
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    BROWN, P
    GOLDFARB, LG
    KOVANEN, J
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    GAJDUSEK, DC
    [J]. ANNALS OF NEUROLOGY, 1992, 31 (03) : 282 - 285
  • [2] NEW MUTATION IN SCRAPIE AMYLOID PRECURSOR GENE (AT CODON-178) IN FINNISH CREUTZFELDT-JAKOB KINDRED
    GOLDFARB, LG
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    KOVANEN, J
    MCCOMBIE, WR
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    [J]. LANCET, 1991, 337 (8738) : 425 - 425
  • [3] JACOB H, 1950, Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr, V184, P653, DOI 10.1007/BF00344941
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  • [5] Two peculiar diseases of the central nervous system after a type of spastic pseudosclerosis (Jakob)
    Kirschbaum, W
    [J]. ZEITSCHRIFT FUR DIE GESAMTE NEUROLOGIE UND PSYCHIATRIE, 1924, 92 : 175 - 220
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