Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
出版年份 2012 全文链接
标题
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 21, Issue 15, Pages 3500-3512
出版商
Oxford University Press (OUP)
发表日期
2012-05-04
DOI
10.1093/hmg/dds161
参考文献
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