MOLECULAR STUDY OF FACTOR VIII GENE IN EGYPTIAN PATIENTS WITH HEMOPHILIA A
Hanan Mohammed Ali Ahmed;
Abstract
Hemophilia A is an X-linked hereditary bleeding disorder caused by deficient or defective coagulation factor VIII. Multiple molecular defects may affect factor VIII gene such as point mutations, premature stop codons, deletions, insertions and inversions.
Other data
| Title | MOLECULAR STUDY OF FACTOR VIII GENE IN EGYPTIAN PATIENTS WITH HEMOPHILIA A | Authors | Hanan Mohammed Ali Ahmed | Keywords | MOLECULAR STUDY OF FACTOR VIII GENE IN EGYPTIAN PATIENTS WITH HEMOPHILIA A | Issue Date | 2009 | Description | Hemophilia A is an X-linked hereditary bleeding disorder caused by deficient or defective coagulation factor VIII. Multiple molecular defects may affect factor VIII gene such as point mutations, premature stop codons, deletions, insertions and inversions. |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 74394r866.pdf | 163.91 kB | Adobe PDF | View/Open |
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