Substrate-specific gene expression profiles in different kidney cell types are associated with Fabry disease

Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the gene encoding the α-galactosidase A (α-Gal A) lysosomal enzyme, which results in globotriaosylceramide (Gb3) storage in vascular endothelial cells and different cell types throughout the body. Involvement of the of Fa...

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Detalles Bibliográficos
Autores principales: SHIN, YOUN-JEONG, JEON, YEO JIN, JUNG, NAMHEE, PARK, JOO-WON, PARK, HAE-YOUNG, JUNG, SUNG-CHUL
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581816/
https://www.ncbi.nlm.nih.gov/pubmed/26135632
http://dx.doi.org/10.3892/mmr.2015.4010

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581816/
https://www.ncbi.nlm.nih.gov/pubmed/26135632
http://dx.doi.org/10.3892/mmr.2015.4010

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