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Acquired modification of sphingosine-1-phosphate lyase activity is not related to adrenal insufficiency

BACKGROUND: Congenital sphingosine-1-phosphate (S1P) lyase deficiency due to biallelic mutations in SGPL1 gene has recently been described in association with primary adrenal insufficiency and steroid-resistant nephrotic syndrome. S1P lyase, on the other hand, is therapeutically inhibited by fingoli...

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Detalles Bibliográficos
Autores principales:	Sunter, Gulin, Enver, Ece Oge, Akbarzade, Azad, Turan, Serap, Vatansever, Pinar, Gunal, Dilek Ince, Haklar, Goncagul, Bereket, Abdullah, Agan, Kadriye, Guran, Tulay
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2018
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5911956/ https://www.ncbi.nlm.nih.gov/pubmed/29685115 http://dx.doi.org/10.1186/s12883-018-1049-9

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