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The <jats:italic>CUBN<\/jats:italic>\u2010related phenotype appears to be dependent upon both variant type and the domain site within the gene. Knowledge of <jats:italic>CUBN<\/jats:italic> status may allow for avoidance of invasive testing.<\/jats:p>","DOI":"10.1002\/ccr3.7502","type":"journal-article","created":{"date-parts":[[2023,6,12]],"date-time":"2023-06-12T08:56:52Z","timestamp":1686560212000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Isolated benign persistent proteinuria with novel association of <i>CUBN<\/i> (cubilin) variants"],"prefix":"10.1002","volume":"11","author":[{"given":"Vivian","family":"Shi","sequence":"first","affiliation":[{"name":"Warren Alpert Medical School of Brown University  Rhode Island Providence USA"},{"name":"Department of Medicine, Rhode Island Hospital  Rhode Island Providence USA"},{"name":"Department of Pediatrics, Hasbro Children\u2019s Hospital  Rhode Island Providence USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7670-9281","authenticated-orcid":false,"given":"Quinn","family":"Stein","sequence":"additional","affiliation":[{"name":"Natera, Inc.  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