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...
Tallennettuna:
| Päätekijät: | , , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMC
2011-06-01
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| Sarja: | Diagnostic Pathology |
| Linkit: | http://www.diagnosticpathology.org/content/6/1/54 |
| Tagit: |
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