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Article

Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitor

19 Apr 2006

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 16638441
DOI: 10.1016/j.bbrc.2006.03.092

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Related research

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Missense mutations in the coagulation factor XII (Hageman factor) gene in hereditary angioedema with normal C1 inhibitorPMID 16638441Read ↗

Hereditary angioedema with normal C1 inhibitor activity including hereditary angioedema with coagulation factor XII gene mutations.Semantic proximity Read ↗

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Hereditary angioedema with normal c1 inhibition.Semantic proximity Read ↗

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C1-inhibitor and its genetic alterations in hereditary angioneurotic edema.Semantic proximity Read ↗

A missense mutation in the plasminogen gene, within the plasminogen kringle 3 domain, in hereditary angioedema with normal C1 inhibitorSemantic proximity Read ↗

Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedemaSemantic proximity Read ↗

Mechanisms involved in hereditary angioedema with normal C1-inhibitor activitySemantic proximity Read ↗

Characterization of a partial exon 9/intron 9 deletion in the coagulation factor XII gene (F12) detected in two Turkish families with hereditary angioedema and normal C1 inhibitor.Semantic proximity Read ↗

Genetic Analysis as a Practical Tool for Diagnosis of Hereditary Angioedema With Normal C1 Inhibitor: A Case Report.Semantic proximity Read ↗

Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.Semantic proximity Read ↗

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