A PRION PROTEIN MISSENSE VARIANT IS INTEGRATED IN KURU PLAQUE CORES IN PATIENTS WITH GERSTMANN-STRAUSSLER SYNDROME

被引：41

作者：

KITAMOTO, T

YAMAGUCHI, K

DOHURA, K

TATEISHI, J

机构：

[1] KYOWA HAKKO KOGYO CO LTD,TOKYO RES LABS,TOKYO,JAPAN

[2] KYUSHU UNIV,DEPT NEUROPATHOL,FUKUOKA 812,JAPAN

来源：

NEUROLOGY | 1991年 / 41卷 / 02期

关键词：

D O I：

10.1212/WNL.41.2_Part_1.306

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：306 / 310

页数：5

共 35 条

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[6] PRO-]LEU CHANGE AT POSITION-102 OF PRION PROTEIN IS THE MOST COMMON BUT NOT THE SOLE MUTATION RELATED TO GERSTMANN-STRAUSSLER SYNDROME
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[7] CREUTZFELDT-JAKOB DISEASE PATIENTS WITH CONGOPHILIC KURU PLAQUES HAVE THE MISSENSE VARIANT PRION PROTEIN COMMON TO GERSTMANN-STRAUSSLER SYNDROME
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