In Silico Study of Correlation between Missense Variations of F8 Gene and Inhibitor Formation in Severe Hemophilia A
Objective: Deleterious substitutions of the F8 gene are responsible for causing hemophilia A, which is an inherited bleeding disorder resulting from reduced or absent activity of the coagulant protein factor VIII (FVIII). The most important complication in treatment is inhibitor development toward t...
محفوظ في:
| المؤلفون الرئيسيون: | , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Turkish Society of Hematology
2020-05-01
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| سلاسل: | Turkish Journal of Hematology |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-09633 |
| الوسوم: |
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