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The natural history of 21-hydroxylase autoantibodies in autoimmune Addison’s disease
BACKGROUND: The most common cause of primary adrenal failure (Addison’s disease) in the Western world is autoimmunity characterized by autoantibodies against the steroidogenic enzyme 21-hydroxylase (CYP21A2, 21OH). Detection of 21OH-autoantibodies is currently used for aetiological diagnosis, but ho...
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| Publicado no: | Eur J Endocrinol |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Bioscientifica Ltd
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8052519/ https://ncbi.nlm.nih.gov/pubmed/34665570 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EJE-20-1268 |
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