Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.

Background: More than 30 genes can harbor rare exonic variants sufficient to cause nephrotic syndrome (NS), and the number of genes implicated in monogenic NS continues to grow. However, outside the first year of life, the majority of affected patients, particularly in ancestrally mixed populations,...

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Bibliographic Details

Published in:	Pediatric Nephrology Vol. 32; no. 3; pp. 467 - 477
Main Authors:	Crawford, Brendan, Gillies, Christopher, Robertson, Catherine, Kretzler, Matthias, Otto, Edgar, Vega-Wagner, Virginia, Sampson, Matthew
Format:	research tables/charts Journal Article
Published:	Springer Nature Mar2017
Online Access:	View this record in EBSCOhost