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Identifying the genetic causes of ataxias using Next-generation sequencing (NGS) methods.

Identifying the genetic causes of ataxias using Next-generation sequencing (NGS) methods.
使用新一代测序 (NGS) 方法识别共济失调的遗传原因。
批准号:
318747
负责人:
Tetreault Martine
金额:
$9.83万
依托单位:
依托单位国家:
加拿大
项目类别:
Fellowship Programs
财政年份:
2014
资助国家:
加拿大
项目状态:
已结题
起止时间:
2014-11-01 至 2017-11-01

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中文摘要
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英文摘要
The human genome is made up of approximately 22,000 functional units known as genes. Mutations in these genes can cause thousands rare but nonetheless serious diseases impacting hundreds of thousands of Canadians. Many of those rare diseases are affecting
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