Associated Papers
Hereditary angioedema due to C1 inhibitor deficiency in Belarus: epidemiology, access to diagnosis and seven novel mutations in SERPING1 gene.
Guryanova I et al.
Clinical and Molecular Allergy : Cma, 2021
Hereditary angioedema caused by a premature stop codon mutation in the SERPING1 gene.
Xu YY et al.
Clinical and Translational Allergy, 2020
Hereditary angioedema: a Chinese perspective.
Liu S et al.
European Journal of Dermatology : Ejd, 2019
Hereditary Angioedema Due to C1 Inhibitor Deficiency in Serbia: Two Novel Mutations and Evidence of Genotype-Phenotype Association.
Andrejević S et al.
Plos One, 2015
Mutational spectrum and geno-phenotype correlation in Chinese families with hereditary angioedema.
Xu YY et al.
Allergy, 2012
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