F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

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Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association Genetics of Hereditary Angioedema Revisited."Nuts and Bolts" of Laboratory Evaluation of Angioedema.Pediatric hereditary angioedema: an update.

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F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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name

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

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F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

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Item

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F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

@en

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

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prefLabel

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

@en

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

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P1476

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

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P2860

Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III

2010 International consensus algorithm for the diagnosis, therapy and management of hereditary angioedema.

Clinical practice. Hereditary angioedema.

Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III

Management of hereditary angioedema in pediatric patients.

Current update on cellular and molecular mechanisms of hereditary angioedema.

Bradykinin and the pathogenesis of hereditary angioedema.

Hereditary angioedema with normal C1-INH with versus without specific F12 gene mutations.

Association of the factor XII 46C>T polymorphism with risk of coronary heart disease (CHD) in the WOSCOPS study.

Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.

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F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

about

P2860

P2860

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.

description

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P1433

P1476

P2093

P2860

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