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
Novel factor VII gene mutations in six families with hereditary coagulation factor VII deficiency.
Zhang X et al.
Journal of Clinical Laboratory Analysis, 2021
[Analysis of the gene mutation in an inherited FVII deficiency patient].
Li R et al.
Zhonghua Yi Xue Za Zhi, 2015
Using a minigene approach to characterize a novel splice site mutation in human F7 gene causing inherited factor VII deficiency in a Chinese pedigree.
Yu T et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2009
[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
Select a paper to view details