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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...
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| Главные авторы: | , , |
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| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Dove Medical Press
2013
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3674014/ https://ncbi.nlm.nih.gov/pubmed/23761984 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/JBM.S32693 |
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