Associated Papers
Factor VII deficiency in China: Phenotype, genotype and current status of management.
Qu C et al.
British Journal of Haematology, 2023
Compound Heterozygous Mutations in the F7 Gene in 2 Unrelated Families With Congenital Factor VII Deficiency.
Ma C et al.
Journal of Pediatric Hematology/oncology, 2021
[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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