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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Detalles Bibliográficos
Autores principales: Sajjadi-Jazi, Sayed Mahmoud, Soltani, Akbar, Enayati, Samaneh, Kakavand Hamidi, Armita, Amoli, Mahsa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698041/
https://www.ncbi.nlm.nih.gov/pubmed/31420020
http://dx.doi.org/10.1186/s12881-019-0870-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698041/
https://www.ncbi.nlm.nih.gov/pubmed/31420020
http://dx.doi.org/10.1186/s12881-019-0870-3

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