发明名称 |
POLYMORPHISM IN A NITRIC OXIDE SYNTHASE GENE |
摘要 |
A method of diagnosis of disease or predisposition to disease, in particular Syndrome X or a component thereof such as hypertension, comprising genotyping an inducible nitric oxide synthase gene. The presence of a four base insertion polymorphism in the promoter region of said gene denotes an individual with increased risk of disease, in particular hypertension and/or the group of conditions known as Syndrome X. |
申请公布号 |
EP1078103(A1) |
申请公布日期 |
2001.02.28 |
申请号 |
EP19990922275 |
申请日期 |
1999.05.07 |
申请人 |
GEMINI GENOMICS (UK) LIMITED |
发明人 |
GRIFFITHS, LYNETTE, ROBYN |
分类号 |
C12Q1/68;(IPC1-7):C12Q1/68 |
主分类号 |
C12Q1/68 |
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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