NEW MUTATION IN SCRAPIE AMYLOID PRECURSOR GENE (AT CODON-178) IN FINNISH CREUTZFELDT-JAKOB KINDRED

被引：156

作者：

GOLDFARB, LG

HALTIA, M

BROWN, P

NIETO, A

KOVANEN, J

MCCOMBIE, WR

TRAPP, S

GAJDUSEK, DC

机构：

[1] NINCDS,MOLEC & CELLULAR NEUROBIOL LAB,RECEPTOR BIOCHEM & MOLEC BIOL SECT,BETHESDA,MD 20892

[2] UNIV HELSINKI,DEPT PATHOL,SF-00100 HELSINKI 10,FINLAND

[3] UNIV HELSINKI,DEPT NEUROL,SF-00100 HELSINKI 10,FINLAND

来源：

LANCET | 1991年 / 337卷 / 8738期

关键词：

D O I：

10.1016/0140-6736(91)91198-4

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：425 / 425

页数：1

共 8 条

[1] CREUTZFELDT-JAKOB DISEASE OF LONG DURATION - CLINICOPATHOLOGICAL CHARACTERISTICS, TRANSMISSIBILITY, AND DIFFERENTIAL-DIAGNOSIS
BROWN, P
RODGERSJOHNSON, P
CATHALA, F
GIBBS, CJ
GAJDUSEK, DC
[J]. ANNALS OF NEUROLOGY, 1984, 16 (03) : 295 - 304
[2] MUTATION IN CODON-200 OF SCRAPIE AMYLOID PROTEIN GENE IN 2 CLUSTERS OF CREUTZFELDT-JAKOB DISEASE IN SLOVAKIA
GOLDFARB, LG
MITROVA, E
BROWN, P
TOH, BH
GAJDUSEK, DC
[J]. LANCET, 1990, 336 (8713) : 514 - 515
[3] MUTATION IN CODON-200 OF SCRAPIE AMYLOID PRECURSOR GENE LINKED TO CREUTZFELDT-JAKOB DISEASE IN SEPHARDIC JEWS OF LIBYAN AND NON-LIBYAN ORIGIN
GOLDFARB, LG
KORCZYN, AD
BROWN, P
CHAPMAN, J
GAJDUSEK, DC
[J]. LANCET, 1990, 336 (8715) : 637 - 638
[4] MUTATIONS IN FAMILIAL CREUTZFELDT-JAKOB DISEASE AND GERSTMANN-STRAUSSLER-SCHEINKERS SYNDROME
GOLDGABER, D
GOLDFARB, LG
BROWN, P
ASHER, DM
BROWN, WT
LIN, S
TEENER, JW
FEINSTONE, SM
RUBENSTEIN, R
KASCSAK, RJ
BOELLAARD, JW
GAJDUSEK, DC
[J]. EXPERIMENTAL NEUROLOGY, 1989, 106 (02) : 204 - 206
[5] LINKAGE OF A PRION PROTEIN MISSENSE VARIANT TO GERSTMANN-STRAUSSLER SYNDROME
HSIAO, K
BAKER, HF
CROW, TJ
POULTER, M
OWEN, F
TERWILLIGER, JD
WESTAWAY, D
OTT, J
PRUSINER, SB
[J]. NATURE, 1989, 338 (6213) : 342 - 345
[6] DESCRIPTIVE EPIDEMIOLOGY OF CREUTZFELDT-JAKOB DISEASE IN FINLAND
KOVANEN, J
HALTIA, M
[J]. ACTA NEUROLOGICA SCANDINAVICA, 1988, 77 (06): : 474 - 480
[7] AN IN-FRAME INSERTION IN THE PRION PROTEIN GENE IN FAMILIAL CREUTZFELDT-JAKOB DISEASE
OWEN, F
POULTER, M
SHAH, T
COLLINGE, J
LOFTHOUSE, R
BAKER, H
RIDLEY, R
MCVEY, J
CROW, TJ
[J]. MOLECULAR BRAIN RESEARCH, 1990, 7 (03): : 273 - 276
[8] IMMUNOCHEMICAL, MOLECULAR GENETIC, AND TRANSMISSION STUDIES ON A CASE OF GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME
TATEISHI, J
KITAMOTO, T
DOHURA, K
SAKAKI, Y
STEINMETZ, G
TRANCHANT, C
WARTER, JM
HELDT, N
[J]. NEUROLOGY, 1990, 40 (10) : 1578 - 1581

← 1 →