Glucocorticoid receptor gene polymorphisms in hereditary angioedema with C1-inhibitor deficiency

BACKGROUND: Hereditary angioedema caused by C1-inhibitor deficiency (C1-INH-HAE) is a rare, autosomal dominant disorder. C1-INH-HAE is characterized by edema–formation, which may occur in response to stress. The individual’s response to stress stimuli is partly genetically determined. Activation of...

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Detalles Bibliográficos
Autores principales: Zotter, Zsuzsanna, Nagy, Zsolt, Patócs, Attila, Csuka, Dorottya, Veszeli, Nóra, Kőhalmi, Kinga Viktória, Farkas, Henriette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223456/
https://www.ncbi.nlm.nih.gov/pubmed/28069032
http://dx.doi.org/10.1186/s13023-016-0552-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223456/
https://www.ncbi.nlm.nih.gov/pubmed/28069032
http://dx.doi.org/10.1186/s13023-016-0552-6

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