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

Thrombosis and haemostasis - 1 Jun 2013

Mulder René, Wiewel-Verschueren Sophie, Meijer Karina, Mulder André B

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PMID: 23494098
DOI: 10.1160/TH12-12-0933

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Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency.PMID 23494098Read ↗

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

Coagulation factor XI: a database of mutations and polymorphisms associated with factor XI deficiency.Semantic proximity Read ↗

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

Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency.Semantic proximity Read ↗

Gene variants in four pedigrees with hereditary coagulation factor XI deficiency and one novel mutation identification.Semantic proximity Read ↗

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

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

Molecular and functional basis of hereditary factor IX defects.Semantic proximity Read ↗

Molecular genetic analysis of factor XI deficiency: identification of five novel gene alterations and the origin of type II mutation in Portuguese families.Semantic proximity Read ↗

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