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Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations
This investigation facilitates a better understanding of inhibitor development, the critical treatment morbidity in HA patients. Furthermore, six novel mutations are reported, which would expand the mutation spectrum of the F8 gene.
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752620/ https://www.ncbi.nlm.nih.gov/pubmed/33363863 http://dx.doi.org/10.1002/ccr3.3294 |