Associated Papers
Clinical and functional characterization of rare compound heterozygous mutations in the SERPINC1 gene causing severe thrombophilia.
Zhang K et al.
Gene, 2024
[Phenotypic and genetic analysis of a pedigree with inherited antithrombin deficiency].
Xu QY et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2020
Two Novel Mutations Cause Hereditary Antithrombin Deficiency in a Chinese Family.
Zhang H et al.
Acta Haematologica, 2020
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