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In Vivo Studies to define the Role of Progranulin Mutations in Frontotemporal Dementia

In Vivo Studies to define the Role of Progranulin Mutations in Frontotemporal Dementia
确定颗粒体蛋白前体突变在额颞叶痴呆中作用的体内研究
批准号:
179543
负责人:
Leavitt Blair R
金额:
$49.48万
依托单位国家:
加拿大
项目类别:
Operating Grants
财政年份:
2009
资助国家:
加拿大
项目状态:
已结题
起止时间:
2009-03-01 至 2014-03-01

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中文摘要
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英文摘要
Much has already been learned from established mouse models of frontotemporal dementia (FTD) that are known to be caused by mutation of the MAPT gene, the first genetic form of FTD identified. In 2006, mutations were identified in the Progranulin gene (PG
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