Factor VIII haplotypes frequencies in Tunisian hemophiliacs A

<p>Abstract</p> <p>Background</p> <p>The development of inhibitors against factor 8 (F8) is the most serious complication of replacement therapy with F8 in children with severe hemophilia. It was suggested that mismatched F8 replacement therapy may be a risk factor for...

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Bibliographic Details
Main Authors: Meddeb Balkis (Author), Zahra Kaouther (Author), Jlizi Asma (Author), Belhedi Nejla (Author), Elmahmoudi Hejer (Author), Elgaaied Amel (Author), Gouider Emna (Author)
Format: Book
Published: BMC, 2011-06-01T00:00:00Z.
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3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available