Deficiency of ALADIN Impairs Redox Homeostasis in Human Adrenal Cells and Inhibits Steroidogenesis

Triple A syndrome is a rare, autosomal recessive cause of adrenal failure. Additional features include alacrima, achalasia of the esophageal cardia, and progressive neurodegenerative disease. The AAAS gene product is the nuclear pore complex protein alacrima-achalasia-adrenal insufficiency neurologi...

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Detalles Bibliográficos
Autores principales: Prasad, R., Metherell, L. A., Clark, A. J., Storr, H. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2013
Materias:
Glucocorticoids-CRH-ACTH-Adrenal
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958737/
https://www.ncbi.nlm.nih.gov/pubmed/23825130
http://dx.doi.org/10.1210/en.2013-1241

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3958737/
https://www.ncbi.nlm.nih.gov/pubmed/23825130
http://dx.doi.org/10.1210/en.2013-1241

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