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Autoimmune polyglandular syndrome type 1: a case report and brief review
Autoimmune polyglandular syndrome (APS) type 1 is a rare autoimmune disorder inherited in an autosomal recessive pattern due to loss of function of the AIRE gene and defective removal of self-reactive T-lymphocytes during the process of thymic T cell maturation. Its manifestation starts early in lif...
Uloženo v:
| Vydáno v: | J Community Hosp Intern Med Perspect |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Taylor & Francis
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6586102/ https://ncbi.nlm.nih.gov/pubmed/31258868 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/20009666.2019.1616523 |
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