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Paper Details

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.
Mol Psychiatry
20
2019
C, LIM-domain containing transcription factors, RING finger LIM domain, RLIM, RLIM RING finger, RLIM missense variants, RLIM variants, RNF12, X, X-linked E3 ubiquitin ligase, X-linked intellectual disability, XLID, amino acid, amino acids, behavior disorder, behavioral anomalies, congenital malformations, mice, patient, rlim, rlim mutant, syndromic X-linked intellectual disability, syndromic XLID, ubiquitin ligase, wild type RLIM, zebrafish, zebrafish rlim
Author NameAffiliation
Benjamin J KellyThe Institute for Genomic Medicine, Nationwide Children's Hospital
Benjamin J KellyThe Institute for Genomic Medicine, Nationwide Children's Hospital
Peter WhiteThe Ohio State University College of Medicine
Peter WhiteThe Institute for Genomic Medicine, Nationwide Children's Hospital
Andreas DufkeInstitute of Medical Genetics and Applied Genomics, University of Tubingen
Daniel C KoboldtThe Ohio State University College of Medicine
Daniel C KoboldtThe Institute for Genomic Medicine, Nationwide Children's Hospital
Nicholas KatsanisCenter for Human Disease Modeling and Departments of Pediatrics and Psychiatry, Duke University
Nicholas KatsanisCenter for Human Disease Modeling and Departments of Pediatrics and Psychiatry, Duke University
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