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This review provides an update on the genes and mutations associated with <jats:styled-content style=\"fixed-case\">SRNS<\/jats:styled-content> along with a suggested approach for genetic testing in patients with <jats:styled-content style=\"fixed-case\">SRNS<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The number of indentified genes associated with <jats:styled-content style=\"fixed-case\">SRNS<\/jats:styled-content> is increasing along with our understanding of their impact on treatment response and risk of recurrence. A systematic approach to genetic testing in patients with <jats:styled-content style=\"fixed-case\">SRNS<\/jats:styled-content> might aid the physician in selecting appropriate treatment.<\/jats:p><\/jats:sec>","DOI":"10.1111\/apa.12317","type":"journal-article","created":{"date-parts":[[2013,6,16]],"date-time":"2013-06-16T12:16:39Z","timestamp":1371384999000},"page":"844-856","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":32,"title":["Genetics of steroid\u2010resistant nephrotic syndrome: a review of mutation spectrum and suggested approach for genetic testing"],"prefix":"10.1111","volume":"102","author":[{"given":"S","family":"Joshi","sequence":"first","affiliation":[{"name":"Department of Clinical Medicine \u2010 The Department of Pediatrics Research Laboratory\u2010A Aarhus University Hospital Aarhus N 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