Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS.
Gbadegesin R; Bartkowiak B; Lavin PJ; Mukerji N; Wu G; Bowling B; Eckel J; Damodaran T; Winn MP; Pediatric Nephrology (Berlin, Germany), 2009, vol. 24, issue 2, p 281, ISSN 0931041x. ISBN 0931041x.

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