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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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| Опубликовано в: : | J Clin Med |
|---|---|
| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
MDPI
2017
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| Предметы: | |
| Online-ссылка: | 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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