A Novel Deletion Mutation of the F8 Gene for Hemophilia A
<b>Background:</b> Hemophilia A (HA) is an X-linked recessive blood coagulation disorder caused by a variety of abnormalities in F8 gene, resulting in the absence of impaired molecule production of factor VIII (FVIII) in the plasma. The genetic testing of the F8 gene encoding FVIII is used for confi...
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| Autori principali: | , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI AG
2022-11-01
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| Serie: | Diagnostics |
| Soggetti: | |
| Accesso online: | https://www.mdpi.com/2075-4418/12/11/2876 |
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