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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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| Publicado no: | Orphanet J Rare Dis |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5223456/ https://ncbi.nlm.nih.gov/pubmed/28069032 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0552-6 |
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