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Catridecacog: a breakthrough in the treatment of congenital factor XIII A-subunit deficiency?
Circulating factor XIII (FXIII) consists of two active (A) and two carrier (B) subunits in tetrameric form. Congenital FXIII deficiency is a rare autosomal-recessive trait that mostly results from an FXIII A-subunit deficiency. Classic coagulation assays, such as prothrombin time or activated partia...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove Medical Press
2014
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4096448/ https://ncbi.nlm.nih.gov/pubmed/25031548 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/JBM.S35395 |
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