Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis

被引：25

作者：

Lampe, J ^{[1
]}

Kitzler, H

Walter, MC

Lochmüller, H

Reichmann, H

机构：

[1] Dresden Univ Technol, Dept Neurol, D-01307 Dresden, Germany

[2] Friedrich Baur Inst, Munich, Germany

来源：

LANCET | 1999年 / 353卷 / 9151期

关键词：

D O I：

10.1016/S0140-6736(98)05208-8

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：465 / 466

页数：2

共 5 条

[1] PRION PROTEIN IS ABNORMALLY ACCUMULATED IN INCLUSION-BODY MYOSITIS [J].

ASKANAS, V ;

BILAK, M ;

ENGEL, WK ;

ALVAREZ, RB ;

TOME, F ;

LECLERC, A .

NEUROREPORT, 1993, 5 (01) :25-28

[2] SIMILAR GENETIC SUSCEPTIBILITY IN IATROGENIC AND SPORADIC CREUTZFELDT-JAKOB-DISEASE [J].

DESLYS, JP ;

MARCE, D ;

DORMONT, D .

JOURNAL OF GENERAL VIROLOGY, 1994, 75 :23-27

[3] HOMOZYGOUS PRION PROTEIN GENOTYPE PREDISPOSES TO SPORADIC CREUTZFELDT-JAKOB DISEASE [J].

PALMER, MS ;

DRYDEN, AJ ;

HUGHES, JT ;

COLLINGE, J .

NATURE, 1991, 352 (6333) :340-342

[4]

SCHAEFFER WJS, 1996, CLIN NEUROPATHOL, V15, P353

[5] DEGENERATION OF SKELETAL-MUSCLE, PERIPHERAL-NERVES, AND THE CENTRAL-NERVOUS-SYSTEM IN TRANSGENIC MICE OVEREXPRESSING WILD-TYPE PRION PROTEINS [J].

WESTAWAY, D ;

DEARMOND, SJ ;

CAYETANOCANLAS, J ;

GROTH, D ;

FOSTER, D ;

YANG, SL ;

TORCHIA, M ;

CARLSON, GA ;

PRUSINER, SB .

CELL, 1994, 76 (01) :117-129

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