Factor VIII Intron 22 Inversion Mutation in Samples of Iraqi Patients with Hemophilia A
Background:Hemophilia A is an X-linked recessive inherited bleeding illness characterized by a lack of procoagulant factor VIII; the factor VIII gene has more than 3000 different mutations, and the most frequent molecular changes in severe hemophilia A are intron 22 and intron 1 inversions (Inv 22 a...
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Wolters Kluwer Medknow Publications
2024-07-01
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| Schriftenreihe: | Medical Journal of Babylon |
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| Online-Zugang: | https://journals.lww.com/10.4103/MJBL.MJBL_1361_23 |
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