Overview of SERPING1 Variations Identified in Hungarian Patients With Hereditary Angioedema

BACKGROUND: Hereditary angioedema (HAE) due to C1-inhibitor (C1-INH) deficiency (C1-INH-HAE) is a rare autosomal dominant disorder, characterized by recurrent, unpredictable edematous symptoms involving subcutaneous, and/or submucosal tissue. C1-INH-HAE may be caused by more than 700 different mutat...

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Detalles Bibliográficos
Autores principales: Szabó, Edina, Csuka, Dorottya, Andrási, Noémi, Varga, Lilian, Farkas, Henriette, Szilágyi, Ágnes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Allergy
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974857/
https://www.ncbi.nlm.nih.gov/pubmed/35386643
http://dx.doi.org/10.3389/falgy.2022.836465

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974857/
https://www.ncbi.nlm.nih.gov/pubmed/35386643
http://dx.doi.org/10.3389/falgy.2022.836465

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