Associated Papers
Structural and functional characterization of novel F7 mutations identified in Chinese factor VII-deficient patients.
Lou C et al.
British Journal of Haematology, 2023
Factor VII deficiency in China: Phenotype, genotype and current status of management.
Qu C et al.
British Journal of Haematology, 2023
Comprehensive Study of Germline Mutations and Double-Hit Events in Esophageal Squamous Cell Cancer.
Zeng B et al.
Frontiers in Oncology, 2021
33889545 (PubMed )
Supplement: Table_5.XLSX › Sheet1
[Analysis of the gene mutation in an inherited FVII deficiency patient].
Li R et al.
Zhonghua Yi Xue Za Zhi, 2015
[Genetic diagnosis and bioinformatic analysis of a pedigree with inherited factor VII deficiency].
Guo Z et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 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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