Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients
出版年份 2017 全文链接
标题
Progranulin-mediated deficiency of cathepsin D results in FTD and NCL-like phenotypes in neurons derived from FTD patients
作者
关键词
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出版物
HUMAN MOLECULAR GENETICS
Volume 26, Issue 24, Pages 4861-4872
出版商
Oxford University Press (OUP)
发表日期
2017-09-23
DOI
10.1093/hmg/ddx364
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