IDENTICAL MUTATION IN UNRELATED PATIENTS WITH CREUTZFELDT-JAKOB DISEASE

被引:87
作者
GOLDFARB, LG [1 ]
BROWN, P [1 ]
GOLDGABER, D [1 ]
GARRUTO, RM [1 ]
YANAGIHARA, R [1 ]
ASHER, DM [1 ]
GAJDUSEK, DC [1 ]
机构
[1] SUNY STONY BROOK,DEPT PSYCHIAT,STONY BROOK,NY 11794
关键词
D O I
10.1016/0140-6736(90)91693-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:174 / 175
页数:2
相关论文
共 9 条
[1]   LINKAGE OF PRION PROTEIN AND SCRAPIE INCUBATION-TIME GENES [J].
CARLSON, GA ;
KINGSBURY, DT ;
GOODMAN, PA ;
COLEMAN, S ;
MARSHALL, ST ;
DEARMOND, S ;
WESTAWAY, D ;
PRUSINER, SB .
CELL, 1986, 46 (04) :503-511
[2]   DIAGNOSIS OF GERSTMANN-STRAUSSLER SYNDROME IN FAMILIAL DEMENTIA WITH PRION PROTEIN GENE ANALYSIS [J].
COLLINGE, J ;
HARDING, AE ;
OWEN, F ;
POULTER, M ;
LOFTHOUSE, R ;
BOUGHEY, AM ;
SHAH, T ;
CROW, TJ .
LANCET, 1989, 2 (8653) :15-17
[3]   PRO-]LEU CHANGE AT POSITION-102 OF PRION PROTEIN IS THE MOST COMMON BUT NOT THE SOLE MUTATION RELATED TO GERSTMANN-STRAUSSLER SYNDROME [J].
DOHURA, K ;
TATEISHI, J ;
SASAKI, H ;
KITAMOTO, T ;
SAKAKI, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (02) :974-979
[4]  
GOLDFARB LG, IN PRESS EXP NEUROL
[5]   MUTATIONS IN FAMILIAL CREUTZFELDT-JAKOB DISEASE AND GERSTMANN-STRAUSSLER-SCHEINKERS SYNDROME [J].
GOLDGABER, D ;
GOLDFARB, LG ;
BROWN, P ;
ASHER, DM ;
BROWN, WT ;
LIN, S ;
TEENER, JW ;
FEINSTONE, SM ;
RUBENSTEIN, R ;
KASCSAK, RJ ;
BOELLAARD, JW ;
GAJDUSEK, DC .
EXPERIMENTAL NEUROLOGY, 1989, 106 (02) :204-206
[6]  
HSIAO K, 1989, NATURE, V338, P34
[7]   LINKAGE OF THE GENE FOR THE SCRAPIE-ASSOCIATED FIBRIL PROTEIN (PRP) TO THE SIP GENE IN CHEVIOT SHEEP [J].
HUNTER, N ;
FOSTER, JD ;
DICKINSON, AG ;
HOPE, J .
VETERINARY RECORD, 1989, 124 (14) :364-366
[8]  
MITROVA E, 1990, UNCONVENTIONAL VIRUS, P19
[9]  
OWEN F, 1989, LANCET, V1, P51