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

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
项目状态：
已结题
起止时间：
2011-02-01 至 2012-02-01
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

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英文摘要
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
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Identification of genes, mechanisms and therapeutic opportunities for spinocerebellar ataxia