HAE patient self-sampling for biomarker establishment

BACKGROUND: Hereditary Angioedema (HAE) is a genetic disorder that leads to frequent angioedema attacks in various parts of the body. In most cases it is caused by pathogenic variants in the SERPING1 gene, coding for C1-Inhibitor (C1-INH). The pathogenic variants in the gene result in reduced C1-INH...

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Detalles Bibliográficos
Autores principales: Förster, Toni M., Magerl, Markus, Maurer, Marcus, Zülbahar, Selen, Zielke, Susanne, Inhaber, Neil, Crocetta, Donatello, Rolfs, Arndt, Skrahina, Volha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478266/
https://www.ncbi.nlm.nih.gov/pubmed/34583739
http://dx.doi.org/10.1186/s13023-021-02021-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478266/
https://www.ncbi.nlm.nih.gov/pubmed/34583739
http://dx.doi.org/10.1186/s13023-021-02021-x

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