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...
সংরক্ষণ করুন:
| প্রধান লেখক: | , |
|---|---|
| বিন্যাস: | Artigo |
| ভাষা: | Inglês |
| প্রকাশিত: |
Turkish Society of Hematology
2020-05-01
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| মালা: | Turkish Journal of Hematology |
| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-09633 |
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