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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 the development of anti-factor...

Ausführliche Beschreibung

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Bibliografische Detailangaben
Hauptverfasser: Meddeb Balkis, Zahra Kaouther, Jlizi Asma, Belhedi Nejla, Elmahmoudi Hejer, Elgaaied Amel, Gouider Emna
Format: Artigo
Sprache:Inglês
Veröffentlicht: BMC 2011-06-01
Schriftenreihe:Diagnostic Pathology
Online-Zugang:http://www.diagnosticpathology.org/content/6/1/54
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