发明名称 |
Mutations associated with iron disorders |
摘要 |
The invention features a method of diagnosing an iron disorder, e.g., hemochromatosis, or a genetic susceptibility to developing such a disorder in a mammal by determining the presence of a mutation in exon 2 or in an intron of an HFE nucleic acid.
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申请公布号 |
US6355425(B1) |
申请公布日期 |
2002.03.12 |
申请号 |
US19990277457 |
申请日期 |
1999.03.26 |
申请人 |
BILLUPS-ROTHENBERG, INC. |
发明人 |
ROTHENBERG BARRY E.;SAWADA-HIRAI RITSUKO;BARTON JAMES C. |
分类号 |
C07K14/705;C12N15/13;C12Q1/68;(IPC1-7):C12Q1/68;C07H21/02 |
主分类号 |
C07K14/705 |
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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