Associated Papers
Clinical and genetic diagnosis of a patient with focal segmental glomerulosclerosis due to a novel variant of the ANLN gene.
Zhang J et al.
Cen Case Reports, 2026
The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes.
Hall G et al.
Journal of the American Society of Nephrology : Jasn, 2018
Genetic basis of adult-onset nephrotic syndrome and focal segmental glomerulosclerosis.
Liu J et al.
Frontiers of Medicine, 2017
Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS.
Gbadegesin RA et al.
Journal of the American Society of Nephrology : Jasn, 2014
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