| 发明名称 |
GENETIC VARIANTS ON CHR 15Q24 AS MARKERS FOR USE IN DIAGNOSIS, PROGNOSIS AND TREATMENT OF EXFOLIATION SYNDROME AND GLAUCOMA |
| 摘要 |
<p>The present invention relates to methods of diagnosing a susceptibility to an ocular disorder, including glaucoma and exfoliation syndrome. The invention provides methods of diagnosing an increased or decreased susceptibility to exfoliation syndrome and glaucoma, and methods for risk assessment, treatment and prognosis. The invention further relates to kits for use in the methods of the invention.</p> |
| 申请公布号 |
KR20100037592(A) |
申请公布日期 |
2010.04.09 |
| 申请号 |
KR20107000501 |
申请日期 |
2008.06.13 |
| 申请人 |
DECODE GENETICS EHF |
发明人 |
THORLEIFSSON GUDMAR;MAGNUSSON KRISTINN P. |
| 分类号 |
C12Q1/68;A61P27/06;C12N15/12;G01N33/68 |
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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