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A novel mutation with Ins C (882-883) of the factor X gene in a Taiwanese Chinese factor X-deficient family.

Thrombosis and haemostasis - 1 Jan 2004

Shen Ming-Ching, Lin Jen-Shiou, Lin David Shin-Yao, Lin Shu-Wha, Lin Bodo

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PMID: 14748350

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Related research

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A novel mutation with Ins C (882-883) of the factor X gene in a Taiwanese Chinese factor X-deficient family.PMID 14748350Read ↗

Factor XI deficiency as a result of a novel Tyr347Stop nonsense mutation in an elderly Japanese woman.Semantic proximity Read ↗

Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.Semantic proximity Read ↗

Genotypes and phenotypes characterization of 17 Iranian patients with inherited factor X deficiency: identification of a novel mutation: Leu487Phe.Semantic proximity Read ↗

Inherited factor X deficiency: molecular genetics and pathophysiology.Semantic proximity Read ↗

Detection and Gene Mutation Analysis of Three Variations in Two Unrelated Chinese Hereditary Coagulation Factor XI Deficiency Families.Semantic proximity Read ↗

Factor XI deficiency with a novel homozygous mutation Trp599Arg near the C-terminal region.Semantic proximity Read ↗

Factors X Nice I and II: two novel missense mutations (Met-40Val and Pro304Ser) in patient with coagulation factor X deficiency.Semantic proximity Read ↗

Genetic analysis in Factor XI deficient patients from central China: identification of one novel and seven recurrent mutations.Semantic proximity Read ↗

A novel c.290G>A mutation in the Factor 11 gene in a Dutch Caucasian family with a Factor XI deficiency.Semantic proximity Read ↗

Two novel factor X gene mutations in a Chinese family with factor X deficiency.Semantic proximity Read ↗

Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency.Semantic proximity Read ↗

Characterization of the genetic basis of FXI deficiency in two Turkish patients.Semantic proximity Read ↗

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