HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort

Rosemary Thomas, Simone Sanna-Cherchi, Bradley A. Warady, Susan L. Furth, Frederick J. Kaskel, Ali G. Gharavi

Research output: Contribution to journalArticlepeer-review

79 Scopus citations

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Medicine & Life Sciences