Title : Dysregulated autophagy contributes to podocyte damage in Fabry's disease.

Pub. Date : 2013

PMID : 23691056






1 Functional Relationships(s)
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1 This X-linked defect results in the accumulation of enzyme substrates with terminally alpha-glycosidically bound galactose, mainly the neutral glycosphingolipid Globotriaosylceramide (Gb3) in various tissues, including the kidneys. Galactose alpha 1,4-galactosyltransferase (P blood group) Homo sapiens