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Factor VIII Intron 22 Inversion in Severe Hemophilia A Patients in Palestine
BACKGROUND: Hemophilia A is an X-linked recessive bleeding disorder caused by mutations in FVIII gene with an incidence of 1 in 5,000 to 10,000 live born males. The Inv22 mutation is a major cause of the disease worldwide, accounting for up to 40%–50% of severe FVIII mutations. The aim of the presen...
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| Publicat a: | Scientifica (Cairo) |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Hindawi
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7533029/ https://ncbi.nlm.nih.gov/pubmed/33062376 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/3428648 |
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