The Use of Intron 22 Mutation in Detection of Haemophilia A Carrier in Patient's Siblings
Amany Saleh Abd Allah;
Abstract
Haemophilia A is the most common inherited bleeding disorder caused by defects in coagulation factor VIII that is encoded by FVIII gene. It is an X-linked recessive disorder (Castaldo et al., 2007). The clinical symptoms consist of recurrent bleeding in m
Other data
| Title | The Use of Intron 22 Mutation in Detection of Haemophilia A Carrier in Patient's Siblings | Other Titles | استخدام الطفرة الوراثية للانترون22 في اكتشاف حاملى مرض الهيموفيليا " أ " من أخوات المرضى | Authors | Amany Saleh Abd Allah | Keywords | The Use of Intron 22 Mutation in Detection of Haemophilia A Carrier in Patient's Siblings | Issue Date | 2012 | Description | Haemophilia A is the most common inherited bleeding disorder caused by defects in coagulation factor VIII that is encoded by FVIII gene. It is an X-linked recessive disorder (Castaldo et al., 2007). The clinical symptoms consist of recurrent bleeding in m |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 116252p7649.pdf | 284.43 kB | Adobe PDF | View/Open |
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