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pubmed-article:19833663pubmed:abstractTextIn Fabry nephropathy, alpha-galactosidase deficiency leads to accumulation of glycosphingolipids in all kidney cell types, proteinuria and progressive loss of kidney function.lld:pubmed
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pubmed-article:19833663pubmed:articleTitleScoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN).lld:pubmed
pubmed-article:19833663pubmed:affiliationDepartment of Pathology, Vanderbilt University Medical Center, Nashville, TN, USA. agnes.fogo@vanderbilt.edulld:pubmed
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