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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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Hovedforfatter: Zainab W. Al-Maaroof
Format: Artigo
Sprog:Inglês
Udgivet: Wolters Kluwer Medknow Publications 2024-07-01
Serier:Medical Journal of Babylon
Fag:
factor viii
hemophilia a
inversion 22
Online adgang:https://journals.lww.com/10.4103/MJBL.MJBL_1361_23
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