Associated Papers
In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency.
Loli-Ausejo D et al.
Clinical Reviews in Allergy & Immunology, 2021
Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency.
Loules G et al.
Gene, 2018
Novel and recurrent C1 inhibitor gene mutations in nine Japanese patients with hereditary angioedema.
Iwamoto K et al.
Journal of Dermatological Science, 2012
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