Molecular study of factor VIII gene in Egyptian patients with hemophilia A /
دراسة جزيئية لجين العامل الثامن فى المرضى المصريين المصابين بمرض هيموفيليا ا
Hanan Mohammed Ali Ahmed ; Supervised Hanaa Hamed Arnaout , Hanan Nour Raslan , Heba Mohammed Hassan Abouelew
- Cairo : Hanan Mohamed Ali Ahmed , 2009
- 197 P. : charts , facsimiles ; 25cm
Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology
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