Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism
Frederike L. Harms(Universität Hamburg), Katta M. Girisha(Manipal Academy of Higher Education), Andrew A. Hardigan(University of Alabama at Birmingham), Fanny Kortüm(Universität Hamburg), Anju Shukla(Manipal Academy of Higher Education), Malik Alawi(Leibniz Institute of Virology (LIV)), Ashwin Dalal(Centre for DNA Fingerprinting and Diagnostics), Lauren Brady(McMaster University Medical Centre), Mark A. Tarnopolsky(McMaster University Medical Centre), Lynne M. Bird(University of California San Diego), Sophia Ceulemans(Rady Children's Hospital-San Diego), Martina Bebin(University of Alabama at Birmingham), Kevin M. Bowling(HudsonAlpha Institute for Biotechnology), Susan M. Hiatt(HudsonAlpha Institute for Biotechnology), Edward J. Lose(University of Alabama at Birmingham), Michelle Primiano(Columbia University), Wendy K. Chung(Columbia University), Jane Juusola, Zeynep Coban‐Akdemir(Baylor College of Medicine), Matthew N. Bainbridge(Baylor College of Medicine), Wu‐Lin Charng(Baylor College of Medicine), Margaret Drummond‐Borg(Cook Children's Medical Center), Mohammad K. Eldomery(Baylor College of Medicine), Ayman W. El‐Hattab(Tawam Hospital), Mohammed A. Saleh(King Fahd Medical City), Stéphane Bezieau(Centre Hospitalier Universitaire de Nantes), Benjamin Cogné(Centre Hospitalier Universitaire de Nantes), Bertrand Isidor(Inserm), Sébastien Küry(Centre Hospitalier Universitaire de Nantes), James R. Lupski(Baylor College of Medicine), R Myers(HudsonAlpha Institute for Biotechnology), Gregory M. Cooper(HudsonAlpha Institute for Biotechnology), Kerstin Kutsche(Universität Hamburg)
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