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Autoimmune Polyglandular Syndrome Type 1: a case report
BACKGROUND: Mutations of the autoimmune regulator gene (AIRE), located on chromosome 21q22.3, are recognized as the cause of a rare monogenic organ-specific autoimmune disorder called autoimmune polyglandular syndrome type 1 (APS-1). Three major components of this syndrome include chronic mucocutane...
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| Pubblicato in: | BMC Med Genet |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6698041/ https://ncbi.nlm.nih.gov/pubmed/31420020 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-019-0870-3 |
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