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Leveraging large-scale sequencing to identify and validate genetic influences of movement disorders.

Leveraging large-scale sequencing to identify and validate genetic influences of movement disorders.
利用大规模测序来识别和验证运动障碍的遗传影响。
批准号：
453910
负责人：
Dilliott Allison A
金额：
$10.2万
依托单位：
McGill University
依托单位国家：
加拿大
项目类别：
Fellowship Programs
财政年份：
2021
资助国家：
加拿大
项目状态：
已结题
起止时间：
2021-09-01 至 2023-09-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=453910&lang=en
关键词：
Amyotrophic Lateral Sclerosis Bioinformatics Essential Tremor Functional Gene Sets Gene Burden Analysis Genetics Movement Disorders Neurodegenerative Disease Next-Generation Sequencing Rare Variant Enrichment

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中文摘要
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英文摘要
Movement disorders are a subcategory of neurodegenerative diseases caused by progressive deterioration of brain cells and resulting in muscle weakness, abnormal movements, and/or tremors. The disorders may be rarer, but fatal, such as amyotrophic lateral
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