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Investigating the genetic background of rapid eye movement (REM)-sleep behaviour disorder to predict alpha-synucleinopathies

Investigating the genetic background of rapid eye movement (REM)-sleep behaviour disorder to predict alpha-synucleinopathies
研究快速眼动 (REM) 睡眠行为障碍的遗传背景以预测 α-突触核蛋白病
批准号：
449587
负责人：
Rahmanian Shahrzad
金额：
$1.27万
依托单位：
University of Toronto
依托单位国家：
加拿大
项目类别：
Studentship Programs
财政年份：
2020
资助国家：
加拿大
项目状态：
已结题
起止时间：
2020-12-01 至 2021-12-01
来源：
https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=449587&lang=en
关键词：
Alpha-Synucleinopathies Computational Genomics Genetic Variants High-Throughput Sequencing Neurodegeneration Rem-Sleep Behaviour Disorder Whole Genome Sequencing

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Parkinson's disease, dementia with Lewy bodies, and multiple systems atrophy are collectively known as αlpha-synucleinopathies, which are characterized by aggregation and accumulation of αlpha-synuclein. Neurodegeneration at the time of diagno
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