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A functional assay to classify genetic variants in Lynch syndrome

A functional assay to classify genetic variants in Lynch syndrome
林奇综合征遗传变异分类的功能分析
批准号:
nhmrc : GNT1108179
负责人:
A/Pr Daniel Buchanan
金额:
$24.55万
依托单位:
依托单位国家:
澳大利亚
项目类别:
Project Grants
财政年份:
2016
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2016-01-01 至 2017-12-31

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中文摘要
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英文摘要
At least one person in every 1000 is affected by Lynch syndrome, in which faulty DNA repair machinery causes high rates of cancer. People with Lynch syndrome can have their risk of cancer cut substantially with regular screening. However, we often struggle to understand whether people with 'non-standard' DNA sequences in particular genes actually have Lynch syndrome. This project develops a simple test that will tell clinicians whether a given sequence change relates to Lynch syndrome or not.
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