Identification and characterization of the gene responsible for autosomal dominant spinocerebellar ataxia in the Franco-Ontarian population

法国-安大略人群常染色体显性脊髓小脑共济失调基因的鉴定和表征

• 批准号: 226616
• 负责人: McDonell Laura M
• 金额: $ 1.27万
• 依托单位: Ottawa Hospital Research Institute
• 依托单位国家: 加拿大
• 项目类别: Studentship Programs
• 财政年份: 2011
• 资助国家: 加拿大
• 起止时间: 2011-02-01 至 2012-02-01
• 项目状态: 已结题
• 来源: https://webapps.cihr-irsc.gc.ca/decisions/p/project_details.html?applId=226616&lang=en
• 关键词: Bioinformatics; Franco Ontarian Spinocerebellar Ataxia; Functional Studies; Linkage Studies; Microsatellite Mapping; Neurodegeneration; Neurogenetics; Next Generation Sequencing; Polymerase Chain Reaction; Sanger Sequencing

The cerebellar ataxias are a group of neurodegenerative disorders characterized by the degeneration of the lower posterior part of the brain called the cerebellum. To date, more than 28 different types of spinocerebellar ataxias (SCAs) have been recogni

小脑共济失调是一组神经退行性疾病，其特征在于称为小脑的大脑后下部的变性。到目前为止，已发现超过28种不同类型的脊髓小脑共济失调（SCA），