Method to diagnose hereditary hemochromatosis
US5753438A · kind A · utility
15Cited by
0References
16Claims
0Family size
Assignee
Inventors
Key dates
| Filing date | May 8, 1995 |
| Grant date | May 19, 1998 |
| Priority date | — |
| Expiry date | May 8, 2015 |
Classification
- Technology area (CPC Y)Emerging Cross-Sectional Technologies
- CPC primaryY10S435/81
- WIPO fieldBiotechnology
- WIPO sectorChemistry
Abstract
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.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.