HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort.
Thomas R; Sanna-Cherchi S; Warady BA; Furth SL; Kaskel FJ; Gharavi AG; Pediatric Nephrology (Berlin, Germany), 2011, vol. 26, issue 6, p 897, ISSN 1432198x. ISBN 1432198x.

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