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Factor VII Deficiency: Clinical Phenotype, Genotype and Therapy
Factor VII deficiency is the most common among rare inherited autosomal recessive bleeding disorders, and is a chameleon disease due to the lack of a direct correlation between plasma levels of coagulation Factor VII and bleeding manifestations. Clinical phenotypes range from asymptomatic condition—...
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| Publicado no: | J Clin Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5406770/ https://ncbi.nlm.nih.gov/pubmed/28350321 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm6040038 |
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