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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Main Authors: | Meddeb Balkis (Author), Zahra Kaouther (Author), Jlizi Asma (Author), Belhedi Nejla (Author), Elmahmoudi Hejer (Author), Elgaaied Amel (Author), Gouider Emna (Author) |
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Format: | Book |
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BMC,
2011-06-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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