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A comprehensive analysis of NPHS1 gene mutations in patients with sporadic focal segmental glomerulosclerosis
Focal segmental glomerulosclerosis (FSGS) is still one of the common causes of refractory nephrotic syndrome. Nephrin, encoded by podocyte-specific NPHS1 gene, participated in the pathogenesis of FSGS. The sit...
Citation: BMC Medical Genetics 2019 20:111