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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Detalles Bibliográficos
Autores principales: Napolitano, Mariasanta, Siragusa, Sergio, Mariani, Guglielmo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406770/
https://www.ncbi.nlm.nih.gov/pubmed/28350321
http://dx.doi.org/10.3390/jcm6040038

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5406770/
https://www.ncbi.nlm.nih.gov/pubmed/28350321
http://dx.doi.org/10.3390/jcm6040038

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