发明名称 |
TAQMAN MGB PROBE FOR DETECTING MATERNAL INHERITED MITOCHONDRIAL GENETIC DEAFNESS C1494T MUTATION AND ITS USAGE |
摘要 |
<p>A real-time quantitative MGB probe for detecting C1494T mutation in maternal inherited mitochondrial deafness gene and its usage are disclosed. Taqman mutant and wild-type MGB probes and a pair of primers are designed. Genetype of C1494T mutation in maternal inherited mitochondrial deafness gene is analyzed through real-time quantitative Taqman MGB probe method. Therefore maternal inherited mitochondrial deafness can be diagnosed.</p> |
申请公布号 |
KR20090111268(A) |
申请公布日期 |
2009.10.26 |
申请号 |
KR20087019250 |
申请日期 |
2007.11.02 |
申请人 |
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发明人 |
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分类号 |
C12N15/11;C12Q1/68;G01N33/52 |
主分类号 |
C12N15/11 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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