Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
about
Diagnosis and screening of patients with hereditary angioedema in primary careFine-tune regulation of carboxypeptidase N1 controls vascular patterning during zebrafish development.Kininogen Cleavage Assay: Diagnostic Assistance for Kinin-Mediated Angioedema Conditions.Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment.Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio-oedema.C1 inhibitor function using contact-phase proteases as target: evaluation of an innovative assay.F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.
P2860
Q26748520-925E24A9-59FC-40E0-9850-9E8944153D43Q33687095-39957E7C-2A1F-43B3-8D54-4E6002E1FB30Q36148583-C94995FD-E844-4B70-9CFD-DF9140E26602Q38790498-646FCBFB-7FD4-4FC1-8BA3-6EE2934771B6Q40988824-D0B28D87-B31E-4DA7-93F8-36E34AF1262DQ50444583-568B2DA3-22FB-4881-A2A6-678E91C338ECQ50870747-A12DC6FD-92E4-4179-8042-DA9F521EC3EB
P2860
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
description
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name
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
@en
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
@nl
type
label
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
@en
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
@nl
prefLabel
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
@en
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
@nl
P2093
P2860
P50
P356
P1433
P1476
Hereditary angioedema with F12 mutation: factors modifying the clinical phenotype.
@en
P2093
D Charignon
K Djenouhat
P2860
P304
P356
10.1111/ALL.12515
P577
2014-10-10T00:00:00Z