Yüklüyor......
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...
Kaydedildi:
| Asıl Yazarlar: | , , |
|---|---|
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Dove Medical Press
2013
|
| Konular: | |
| Online Erişim: | 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 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|