American Journal of Transplantation · 2015 · 24 citations · 25 references
MedicineGeneticsMolecular GeneticsKidney TransplantationMedical GeneticsRenal PathophysiologyGenetic DisordersGlomerular DiseasesHereditary Kidney DiseasesHereditary Renal DiseasesNephrotic SyndromeRenal DiseaseFocal Segmental Glomerulosclerosis RecurrenceGenetic Glomerular DisordersHereditary Glomerular DiseasesHereditary Nephrotic SyndromePatch-clamp AnalysisPost-transplant ProteinuriaProteinuria After TransplantationRecurrent Focal Segmental Glomerulosclerosis
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SNPStats: a web tool for the analysis of association studies
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A Mutation in the <i>TRPC6</i> Cation Channel Causes Familial Focal Segmental Glomerulosclerosis
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TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function
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