Lack of F8 mRNA
Hemophilia A (HA) is caused by partial or total deficiency of F8 protein activity. In a small group, about 1.8% of patients with HA, no mutation is found in the F8 gene. Among this group, we report here on one patient with severe HA in whom no mRNA of the F8 gene was detected. Using 2 common polymor...
محفوظ في:
| المؤلف الرئيسي: | El Maarri, Osman (author) |
|---|---|
| مؤلفون آخرون: | Singer, Heike (author), Klein, Claudia (author), Watzka, Mathias (author), Herbiniaux, Brackmann (author), Schroder, Jorg (author), Graw, Jochen (author), Muller, Clemens (author), Schramm, Wolfgang (author), Schwaab, Rainer (author), Haaf, Thomas (author), Hanfland, Peter (author), Oldenburg, Johannes (author) |
| التنسيق: | article |
| منشور في: |
2006
|
| الوصول للمادة أونلاين: | http://hdl.handle.net/10725/6173 https://doi.org/10.1182/blood-2005-09-3702 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php http://www.bloodjournal.org/content/107/7/2759.short |
| الوسوم: |
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