New developments in the management of congenital Factor XIII deficiency
Congenital Factor XIII (FXIII) deficiency is a rare, inherited, autosomal recessive coagulation disorder. Most mutations of this condition are found in the A-subunit with almost half these being missense mutations. Globally, approximately one in three million people suffer from this deficiency. Fact...
| Main Authors: | , , |
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| Format: | Online |
| Language: | English |
| Published: |
Dove Medical Press
2013
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674014/ |