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Congenital factor XI deficiency caused by a novel F11 missense variant: a case report
Hereditary factor XI (FXI) deficiency is a mild bleeding disorder, rare in the general population but relatively common among Ashkenazi Jews. The human F11 gene comprises 15 exons, spanning over 23 kb of the long arm of chromosome 4 (4q35). Homozygotes or compound heterozygotes typically show severe...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Croatian Medical Schools
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7063557/ https://www.ncbi.nlm.nih.gov/pubmed/32118380 http://dx.doi.org/10.3325/cmj.2020.61.62 |