Pleiotropy of Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Phenotypes in Human 16p11.2 Microdeletion Syndrome Is Recapitulated in Mouse Models of Tbx6 Deletion: PO1346

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Bibliographic Details
Published in:Journal of the American Society of Nephrology 2021-10, Vol.32 (10S), p.429-429
Main Authors: Whittemore, Gregory B., Martino, Jeremiah, Lim, Tze Yin, Gupta, Yask, Mendelsohn, Cathy L., Sanna-Cherchi, Simone
Format: Article
Language:English
Online Access:Get full text
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ISSN:1046-6673
DOI:10.1681/ASN.20213210S1429d