Associated Papers
Whole-Exome Sequencing for Molecular Diagnosis of Paediatric Nephrotic Syndrome in Africa: A Call for Implementation.
Gcobo T et al.
Genes, 2025
Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice.
Deltas C et al.
Genes, 2023
Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management.
Bierzynska A et al.
Kidney International, 2017
Three-dimensional electron microscopy reveals the evolution of glomerular barrier injury.
Randles MJ et al.
Scientific Reports, 2016
Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.
Lennon R et al.
Pediatric Nephrology (berlin, Germany), 2015
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