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Paper Details

Mutations in <i>PRDM15</i> Are a Novel Cause of Galloway-Mowat Syndrome.
J Am Soc Nephrol
13
2021
GAMOS, GAMOS-type syndrome, Galloway-Mowat Syndrome, Galloway-Mowat syndrome, Human, Human wild-type PRDM15 RNA, PRDM15, PRDM15 Are, PRDM15 protein, PRDM15 variants, Prdm15, Xenopus, ZNF, brain anomalies, cardiac defects, children, developmental kidney genes, human, human podocytes, humans, isolated nephrotic syndrome, nephropathy, neurodevelopmental defects, proteinuric kidney disease, renal developmental genes, renal failure, skeletal defects, steroid-resistant nephrotic syndrome, zinc
Author NameAffiliation
Shrikant ManeYale University School of Medicine
Richard P LiftonYale University School of Medicine
Richard P LiftonThe Rockefeller University
Richard P LiftonYale University School of Medicine
Richard P LiftonThe Rockefeller University
Ernesto GuccioneInstitute of Molecular and Cell Biology
Ernesto GuccioneMount Sinai Center for Therapeutics Discovery, Departments of Pharmacological Sciences and Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai
Martin ZenkerInstitute of Human Genetics, University Hospital Magdeburg
Friedhelm HildebrandtBoston Children's Hospital, Harvard Medical School
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Release 1.2