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Paper Details

Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Am J Hum Genet
20
2020
CAKUT, Congenital anomalies of the kidney and urinary tract, FOXP1, Human, Syndromic Urinary Tract Malformations, X. tropicalis, ZMYM2, ZMYM2 protein, ZMYM2 proteins, Zmym2, birth defects, chronic kidney disease, developmentally regulated endogenous retrovirus elements, human, mice, renal and craniofacial defects, truncated
Author NameAffiliation
David R FitzPatrickMRC Institute of Genetics & Molecular Medicine, Royal Hospital for Sick Children, The University of Edinburgh
Peter J HulickCenter for Medical Genetics, NorthShore University HealthSystem
Peter J HulickCenter for Medical Genetics, NorthShore University HealthSystem
Hila Milo RasoulyColumbia University
Ali G GharaviColumbia University
Heidi L RehmMassachusetts General Hospital, Broad Institute of MIT and Harvard
Heidi L RehmMassachusetts General Hospital, Broad Institute of MIT and Harvard
Daniel G MacArthurMassachusetts General Hospital, Broad Institute of MIT and Harvard
Daniel G MacArthurMassachusetts General Hospital, Broad Institute of MIT and Harvard
Monkol LekMassachusetts General Hospital, Broad Institute of MIT and Harvard
Richard P LiftonThe Rockefeller University
Richard P LiftonThe Rockefeller University
Shrikant ManeYale University School of Medicine
Brian RaughtPrincess Margaret Cancer Centre, University Health Network & Department of Medical Biophysics, University of Toronto
Mustafa K KhokhaYale University School of Medicine
Friedhelm HildebrandtBoston Children's Hospital, Harvard Medical School
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