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A classification system for cross-reactive material-negative factor XI deficiency
The bleeding disorder associated with factor XI (fXI) deficiency is typically inherited as an autosomal recessive trait. However, some fXI mutations may be associated with dominant disease transmission. FXI is a homodimer, a feature that could allow certain mutations to exert a dominant-negative eff...
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The American Society of Hematology
2005
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1895004/ https://ncbi.nlm.nih.gov/pubmed/15728123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2004-05-1864 |
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