Kankan Su
Nanjing, China
Last Updated: 09/26/2026
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Found 11 publications
Genetic Analysis of a Family With Hereditary Factor V Deficiency Induced by Compound Heterozygous Variants (IVS24+3A>T and p.Asp2222Gly).
Journal: Haemophilia : the official journal of the World Federation of Hemophilia
Published: December 10, 2025
A novel mutation (Ser951LeufsTer8) in F5 gene leads to hereditary coagulation factor V deficiency.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: January 14, 2021
Phenotypic and genetic analysis of a pedigree affected with hereditary FV deficiency due to a novel deletional variant of F5 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 09, 2019
Genetic analysis and clinical features of a pedigree affected with hereditary coagulation factor Ⅶ deficiency caused by compound heterozygotic mutations
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 11, 2019
Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121Arg.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: July 02, 2019
Identification of compound heterozygous mutations of F11 gene in a pedigree affected with heriditary coagulation factor XI deficiency
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 06, 2019
Protein C deficiency (a novel mutation: ala291Thr) with systemic lupus erythematosus leads to the deep vein thrombosis.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: November 16, 2018
Phenotypic and mutational analysis of a pedigree affected with hereditary coagulation factor Ⅴ deficiency
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 14, 2018
A novel mutation (Tyr503Cys) in a severe factor XI deficiency.
Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis
Published: March 15, 2018
Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriage.
Journal: International journal of hematology
Published: May 12, 2017
Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation.
Journal: Hematology (Amsterdam, Netherlands)
Published: February 16, 2017
Showing 1-11 of 11
Last Updated: 09/26/2026