Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency

INTRODUCTION: Hereditary human coagulation factor VII (FVII) deficiency is an inherited autosomal recessive hemorrhagic disease involving mutations in the F7 gene. The sites and types of F7 mutations may influence the coagulation activities of plasma FVII (FVII: C) and severity of hemorrhage symptom...

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Detalles Bibliográficos
Autores principales: Zhang, Xiaoyu, Wang, Shuwen, Leng, Shaoqiu, Feng, Qi, Zhang, Yanqi, Xu, Shuqian, Zhang, Lei, Zhang, Xinsheng, Fang, Yunhai, Peng, Jun, Sheng, Zi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418470/
https://www.ncbi.nlm.nih.gov/pubmed/34342048
http://dx.doi.org/10.1002/jcla.23905

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8418470/
https://www.ncbi.nlm.nih.gov/pubmed/34342048
http://dx.doi.org/10.1002/jcla.23905

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