Catridecacog: a breakthrough in the treatment of congenital factor XIII A-subunit deficiency?

Catridecacog: a breakthrough in the treatment of congenital factor XIII A-subunit deficiency?

Wolfgang Korte1,21Center for Laboratory Medicine, 2Center for Hemostaseology and Hemophilia, St Gallen, SwitzerlandAbstract: 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 tha...

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Bibliographic Details
Main Author:	Korte W
Format:	Article
Language:	English
Published:	Dove Medical Press 2014-07-01
Series:	Journal of Blood Medicine
Online Access:	http://www.dovepress.com/catridecacog-a-breakthrough-in-the-treatment-of-congenital-factor-xiii-a17529

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