Associated Papers
Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency.
Loules G et al.
Gene, 2018
F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema.
Speletas M et al.
Allergy, 2015
The Turkish Hereditary Angioedema Pilot Study (TURHAPS): the first Turkish series of hereditary angioedema.
Kesim B et al.
International Archives of Allergy and Immunology, 2011
Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.
Pappalardo E et al.
Molecular Immunology, 2008
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