Shasha Luo

Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.

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

Published: July 15, 2021

A homozygous variant in a consanguineous pedigree with inherited protein S deficiency

Journal: Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases

Published: April 08, 2021

Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.

Journal: Hamostaseologie

Published: December 29, 2020

Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family.

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

Published: November 16, 2020

Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 14, 2020

A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.

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

Published: August 25, 2020

Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.

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

Published: August 25, 2020

Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 31, 2020

Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr).

Journal: Hamostaseologie

Published: May 26, 2020

Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.

Two heterozygous mutations associated with type I protein C deficiency in two Chinese independent families.

A homozygous variant in a consanguineous pedigree with inherited protein S deficiency

A homozygous variant in a consanguineous pedigree with inherited protein S deficiency

Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.

Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.

Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family.

Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family.

Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene

Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene

A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.

A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.

Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.

Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.

Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene

Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene

Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr).

Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr).

A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patient.

A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patient.

Genetic analysis of a pedigree with hereditary coagulation factor XI deficiency.

Genetic analysis of a pedigree with hereditary coagulation factor XI deficiency.

Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121Arg.

Phenotypic and genetic analysis of hypofibrinogenemia because of a novel missense mutation in the FGB: Leu121Arg.