Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE)

Existing evidence indicates that modifier genes could change the phenotypic outcome of the causal SERPING1 variant and thus explain the expression variability of hereditary angioedema due to C1-inhibitor deficiency (C1-INH-HAE). To further examine this hypothesis, we investigated the presence or abs...

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Detalles Bibliográficos
Autores principales: Parsopoulou, Faidra, Loules, Gedeon, Zamanakou, Maria, Csuka, Dorottya, Szilagyi, Agnes, Kompoti, Maria, Porebski, Grzegorz, Psarros, Fotis, Magerl, Markus, Valerieva, Anna, Staevska, Maria, Obtulowicz, Krystyna, Maurer, Marcus, Speletas, Matthaios, Farkas, Henriette, Germenis, Anastasios E.
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/PMC9300820/
https://www.ncbi.nlm.nih.gov/pubmed/35873600
http://dx.doi.org/10.3389/falgy.2022.868185

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300820/
https://www.ncbi.nlm.nih.gov/pubmed/35873600
http://dx.doi.org/10.3389/falgy.2022.868185

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