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RESEARCH PRODUCT

Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]

Felipe Gonçalves Motta MaiaMaria Luiza Oliva AlonsoKonrad BorkL. Karla ArrudaAdriana S. MorenoSoloni Afra Pires LevyWilson A. SilvaFabrício C. DiasLuana S.m. MaiaMariana Paes Leme FerrianiMaria Fernanda FerraroPérsio Roxo-juniorFaradiba Sarquis SerpaMarina Mendonça DiasDavi Casale AragonAlfeu Tavares FrançaAntonio Abilio MottaSven CichonSven CichonWilly SartiSolange Oliveira Rodrigues ValleFernanda Leonel Nunes

subject

C1 inhibitor deficiencyGenotypeDOENÇAS HEREDITÁRIASImmunologyBradykininC1-inhibitorchemistry.chemical_compoundmedicineImmunology and AllergyHumansGenotype-Phenotype CorrelationsGenetic Association StudiesbiologyHereditary Angioedema Types I and IIbusiness.industrymedicine.diseaseComplement (complexity)PhenotypechemistryHereditary angioedemaImmunologyMutationbiology.proteinbusinessComplement C1 Inhibitor ProteinBrazil
yearjournalcountryeditionlanguage
2019-01-22
10.1111/all.13699
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