Mutant prion protein D202N associated with familial prion disease is retained in the endoplasmic reticulum and forms ‘curly’ intracellular aggregates 期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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Mutant prion protein D202N associated with familial prion disease is retained in the endoplasmic reticulum and forms ‘curly’ intracellular aggregates

作者姓名：	Gu Y Verghese S Bose S Mohan M Singh N

摘要：
收稿时间：	8 February 2007
修稿时间：	13 February 2007
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