Associated Papers
Inherited coagulation factor VII deficiency in Taiwan: Two novel F7 variants with relevant regional features in 33 patients.
Lin HY et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2024
Factor VII deficiency in China: Phenotype, genotype and current status of management.
Qu C et al.
British Journal of Haematology, 2023
Molecular Characterization of Two Homozygous Factor VII Variants Associated with Intracranial Bleeding.
Andersen E et al.
Thrombosis and Haemostasis, 2021
The EAHAD blood coagulation factor VII variant database.
Giansily-Blaizot M et al.
Human Mutation, 2020
[Analysis of the gene mutation in an inherited FVII deficiency patient].
Li R et al.
Zhonghua Yi Xue Za Zhi, 2015
[Analysis of an inherited FVII deficiency pedigree caused by homozygosity of Thr359Met].
Chu HY et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2003
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