Ke Zhang

Key Laboratory Of Clinical Laboratory Diagnosis And Translational Research Of Zhejiang Province
Wenzhou, China

Last Updated: 09/26/2026

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Found 9 publications

Two patients with protein S deficiency and cerebral venous sinus thrombosis: nonsense mutations of the PROS1 gene may account for these deficiencies.

Two patients with protein S deficiency and cerebral venous sinus thrombosis: nonsense mutations of the PROS1 gene may account for these deficiencies.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: September 30, 2024

Molecular and clinical characterization of two independent Chinese families with protein C deficiency.

Molecular and clinical characterization of two independent Chinese families with protein C deficiency.

Journal: Annals of hematology

Published: May 05, 2024

The spectrum of factor XI deficiency in Southeast China: four recurrent variants can explain most of the deficiencies.

The spectrum of factor XI deficiency in Southeast China: four recurrent variants can explain most of the deficiencies.

Journal: Orphanet journal of rare diseases

Published: February 13, 2024

Clinical and functional characterization of rare compound heterozygous mutations in the SERPINC1 gene causing severe thrombophilia.

Clinical and functional characterization of rare compound heterozygous mutations in the SERPINC1 gene causing severe thrombophilia.

Journal: Gene

Published: September 19, 2023

Clinical Characterization and Molecular Analysis of Fourteen Chinese Patients with Factor V Deficiency.

Clinical Characterization and Molecular Analysis of Fourteen Chinese Patients with Factor V Deficiency.

Journal: Hamostaseologie

Published: September 15, 2023

Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations.

Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations.

Journal: Hamostaseologie

Published: June 15, 2023

Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*).

Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*).

Journal: Blood cells, molecules & diseases

Published: June 11, 2023

Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency.

Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency.

Journal: Annals of hematology

Published: May 22, 2023

Molecular mechanism analysis of a family with hereditary coagulation FXI deficiency caused by compound heterozygous mutations.

Molecular mechanism analysis of a family with hereditary coagulation FXI deficiency caused by compound heterozygous mutations.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: October 05, 2022

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Last Updated: 09/26/2026