Case Report: The Monogenic Familial Steroid-Resistant Nephrotic Syndrome Caused by a Novel Missense Mutation of NPHS2 Gene A593C in a Chinese Family

Overview of attention for article published in Frontiers in Pediatrics, September 2021

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New Research: Case Report: The Monogenic Familial Steroid-Resistant Nephrotic Syndrome Caused by a Novel Missense Mutation of NPHS2 Gene A593C in a Chinese Family: Background: Pathogenic variants in the NPHS2 gene encoding podocin in kidney… https://t.co/c

16 Oct 2021

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