Molecular mechanism of type I congenital heparin cofactor (HC) II deficiency caused by a missense mutation at reactive P2 site: HC II Tokushima (Q32007490)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Molecular mechanism of type I congenital heparin cofactor (HC) II deficiency caused by a missense mutation at reactive P2 site: HC II Tokushima |
scientific article |
Statements
1 reference
Molecular mechanism of type I congenital heparin cofactor (HC) II deficiency caused by a missense mutation at reactive P2 site: HC II Tokushima (English)
1 reference
Kanagawa Y
1 reference
Shigekiyo T
1 reference
Aihara K
1 reference
Akaike M
1 reference
Azuma H
1 reference
Matsumoto T
1 reference
1 January 2001
1 reference
1 reference
101-107
1 reference
Identifiers
1 reference