주의력결핍 과잉행동장애의 진단용 SNP와 그를 포함하는 마이크로어레이 및 키트
    12.
    发明授权
    주의력결핍 과잉행동장애의 진단용 SNP와 그를 포함하는 마이크로어레이 및 키트 有权
    用于诊断多动症,微阵列和包括其的单元,以及使用其诊断ADHD的方法

    公开(公告)号:KR101157526B1

    公开(公告)日:2012-06-22

    申请号:KR1020110094918

    申请日:2011-09-20

    CPC classification number: C12Q1/6883 C12Q2600/156 G01N21/76 C12Q1/6844

    Abstract: PURPOSE: A composition for diagnosing risk of developing ADHD and a kit are provided to classify a risk group of developing ADHD and to prevent ADHA. CONSTITUTION: A composition for diagnosing ADHA contains a polynucleotide of rs550818 SNP in GIT gene having24926101th C/T base of 17th human chromosome. The composition contains likage disequilibrium site near the rs550818 SNP. A method for predicting risk of developing ADHD comprises: a step of isolating DNAs from a biological sample of a subject; a step of identifying the rs550818 SNP base at 24926101th base site in 17th human chromosome; and a step of determining high risk of developing ADHD in case that the rs550818 SNP allele is C/T.

    Abstract translation: 目的:提供一种用于诊断发展中ADHD风险的组合物和一个试剂盒,用于分类发展中的ADHD的风险组并防止ADHA。 构成:用于诊断ADHA的组合物含有GIT基因中rs550818 SNP的多核苷酸,其具有第17个人染色体的第24926101个C / T碱基。 该组合物包含rs550818 SNP附近的可能不平衡位点。 用于预测发展中的ADHD的风险的方法包括:从受试者的生物样品中分离DNA的步骤; 在第17个人类染色体的第24926101个碱基位点鉴定rs550818 SNP碱基的步骤; 并且在rs550818 SNP等位基因为C / T的情况下确定发生ADHD的高风险的步骤。

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