Methylene tetrahydrofolate reductase gene mutation; A1298C and its relation to coronary artery disease
Rasha Tharwat Mohamed Ali;
Abstract
Thrombophilia is an increased risk of thrombosis hereditary or acquired. The hereditary causes of thrombophilia are deficiency of PC, PS and antithrombin III, factor V Leiden, hyperhomocysteinaemia, prothrombin G20210A polymorphism and elevated levels of
Other data
| Title | Methylene tetrahydrofolate reductase gene mutation; A1298C and its relation to coronary artery disease | Other Titles | طفرﺓ جين مختزل الميثيل تيتراهيدروفوليت A1298C و علاقته بأمراض الشريان التاجي | Authors | Rasha Tharwat Mohamed Ali | Keywords | Methylene tetrahydrofolate reductase gene mutation; A1298C and its relation to coronary artery disease | Issue Date | 2010 | Description | Thrombophilia is an increased risk of thrombosis hereditary or acquired. The hereditary causes of thrombophilia are deficiency of PC, PS and antithrombin III, factor V Leiden, hyperhomocysteinaemia, prothrombin G20210A polymorphism and elevated levels of |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 99838p1498.pdf | 783.79 kB | Adobe PDF | View/Open |
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