| 发明名称 |
Method to diagnose hereditary hemochromatosis |
| 摘要 |
New genetic markers for the presence of a mutation in the common hereditary hemochromatosis (HH) gene are disclosed. The multiplicity of markers permits definition of genotypes characteristic of carriers and homozygotes containing this mutation in their genomic DNA. |
| 申请公布号 |
AU722885(B2) |
申请公布日期 |
2000.08.10 |
| 申请号 |
AU19960058559 |
申请日期 |
1996.05.08 |
| 申请人 |
BIO-RAD LABORATORIES, INC. |
发明人 |
DENNIS T. DRAYNA;JOHN N. FEDER;ANDREAS GNIRKE;BRUCE E. KIMMEL;WINSTON J. THOMAS;ROGER K. WOLFF |
| 分类号 |
C12Q1/68;(IPC1-7):C12P19/34;C07H21/04 |
主分类号 |
C12Q1/68 |
| 代理机构 |
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代理人 |
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