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Possible role of transforming growth factor-β1 and vascular endothelial growth factor in Fabry disease nephropathy

Fabry disease is a lysosomal storage disorder (LSD) caused by deficiency of α-galactosidase A (α-gal A), resulting in deposition of globotriaosylceramide (Gb3; also known as ceramide trihexoside) in the vascular endothelium of many organs. A gradual accumulation of Gb3 leads to cardiovascular, cereb...

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Detalles Bibliográficos
Autores principales:	LEE, MI HEE, CHOI, EUN NAM, JEON, YEO JIN, JUNG, SUNG-CHUL
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2012
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042857/ https://www.ncbi.nlm.nih.gov/pubmed/23007467 http://dx.doi.org/10.3892/ijmm.2012.1139

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