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Focal segmental glomerulosclerosis and proteinuria associated with Myo1E mutations: novel variants and histological phenotype analysis

Mira Krendel, Sabine Leh, Michael E. Garone, Alcia Edwards-Richards, Jen‐Jar Lin, Damien Brackman, Per M. Knappskog, Alexei Mikhailov

2022Pediatric Nephrology16 citationsDOIOpen Access PDF

Topics & Concepts

Alport syndromeFocal segmental glomerulosclerosisPodocytePodocinGlomerular basement membraneSlit diaphragmNephrotic syndromeGlomerulosclerosisNephrologyActin cytoskeletonPhenotypeMedicinePathologyNephrinGlomerulonephritisGeneticsBiologyInternal medicineKidneyProteinuriaGeneCytoskeletonCellRenal Diseases and GlomerulopathiesCell Adhesion Molecules ResearchRenal and related cancers
Focal segmental glomerulosclerosis and proteinuria associated with Myo1E mutations: novel variants and histological phenotype analysis | Litcius