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Article

Severe factor VII deficiency caused by a novel point mutation (Arg353Pro) combined with a rare Cys22Arg mutation.

Thrombosis and haemostasis - 1 Sept 2007

Zhidong Wang, Xiaojun Huang

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 17849063

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Severe factor VII deficiency caused by a novel point mutation (Arg353Pro) combined with a rare Cys22Arg mutation.PMID 17849063Read ↗

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A novel factor X mutation Cys81 by Arg and a reported factor VII polymorphism Arg353 replaced by Gln co-occured in a patient.Semantic proximity Read ↗

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

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Identification of four novel mutations in the factor VIII gene: three missense mutations (E1875G, G2088S, I2185T) and a 2-bp deletion (1780delTC).Semantic proximity Read ↗

Molecular basis of hereditary factor VII deficiency in India: five novel mutations including a double missense mutation (Ala191Glu; Trp364Cys) in 11 unrelated patients.Semantic proximity Read ↗

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Novel Mutation p.Asp374Val of SERPINC1 in a Turkish Family with Inherited Antithrombin DeficiencySemantic proximity Read ↗

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

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