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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: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096448/ https://www.ncbi.nlm.nih.gov/pubmed/25031548 http://dx.doi.org/10.2147/JBM.S35395 |