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Paper Details

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction.
Am J Hum Genet
25
2021
Author NameAffiliation
Alexander J M Dingemansthe Netherlands Donders Institute for Brain, Radboud University
Christoffer Nell??kerUniversity of Oxford, John Radcliffe Hospital, UK Institute of Biomedical Engineering, UK Big Data Institute
Siddharth BankaUniversity of Manchester, St Mary's Hospital, Manchester University NHS Foundation Trust
Han G Brunnerthe Netherlands Donders Institute for Brain, Radboud University, the Netherlands Maastricht University Medical Center
Jacqueline ChrastCenter for Integrative Genomics, University of Lausanne
Hilary CoonUniversity of Utah School of Medicine
Christian Gilissenthe Netherlands Radboud Institute for Molecular Life Sciences, Radboud University Medical Center
Jayne Y Hehir-KwaPrincess Maxima Center for Pediatric Oncology
Pengfei LiuBaylor College of Medicine
Mohamad A MikatiDuke University Medical Center
Shehla MohammedClinical Genetics, Guy's Hospital
Kelly RadtkeClinical Genomics Department
Rebecca C SpillmannDuke University Medical Center
Alexandre ReymondCenter for Integrative Genomics, University of Lausanne
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