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Rare congenital bleeding disorders
The rare congenital bleeding disorders are a heterogeneous group of diseases which include deficiencies of fibrinogen, prothrombin and factors V, V + VIII, VII, X, XI and XIII. They are usually transmitted as autosomal recessive disorders, and the prevalence of the severe forms ranges from one case...
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| Pubblicato in: | Ann Transl Med |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
AME Publishing Company
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6174186/ https://ncbi.nlm.nih.gov/pubmed/30306070 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2018.08.34 |
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