Prion diseases

被引：83

作者：

Knight, RSG ^{[1
]}

Will, RG ^{[1
]}

机构：

[1] Western Gen Hosp, Natl CJD Surveillance Unit, Edinburgh EH4 2XU, Midlothian, Scotland

来源：

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY | 2004年 / 75卷

关键词：

D O I：

10.1136/jnnp.2004.036137

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Prion diseases or transmissible spongiform encephalopathies (table 1) are characterised by the deposition of PrPSc, an abnormal form of a normal cellular protein, PrPC. These diseases exist in sporadic (idiopathic), genetic, and acquired forms.

引用

页码：I36 / I42

页数：7

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