Correction: Olfactory bulb anomalies in KBG syndrome mouse model and patients

Affiliations

• ¹ Department of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, T6G 2H7, Canada.
• ² Women and Children's Health Research Institute, University of Alberta, 5‑083 Edmonton Clinic Health Academy, Edmonton, AB, T6G 1C9, Canada.
• ³ Clinical Genetics Service and Coordination Center for Rare Diseases, Department of Pediatrics, Regional Hospital of Bolzano, Bolzano, Italy.
• ⁴ Clinical Genetics Unit, Hopital Robert-Debre, Paris, France.
• ⁵ IRCCS Istituto Delle Scienze Neurologiche Di Bologna, UOC Neuropsichiatria Dell'eta Pediatrica, Bologna, Italy.
• ⁶ Programma Di Neuroradiologia Con Tecniche Ad Elevata Complessita (PNTEC), IRCCS Istituto Delle Scienze Neurologiche Di Bologna, Bologna, Italy.
• ⁷ Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesu Children's Hospital, IRCCS, 00165, Rome, Italy.
• ⁸ Service d'Imagerie Pediatrique, Hopital Universitaire Robert Debre, Paris, France.
• ⁹ Department of Academic Child Health, Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
• ¹⁰ Clinical Genetics Service, St. Michaels Hospital, Bristol, UK.
• ¹¹ Department of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, T6G 2H7, Canada. voronova@ualberta.ca.
• ¹² Women and Children's Health Research Institute, University of Alberta, 5‑083 Edmonton Clinic Health Academy, Edmonton, AB, T6G 1C9, Canada. voronova@ualberta.ca.
• ¹³ Department of Cell Biology, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, T6G 2H7, Canada. voronova@ualberta.ca.
• ¹⁴ Faculty of Medicine & Dentistry, Neuroscience and Mental Health Institute, Edmonton, AB, T6G 2E1, Canada. voronova@ualberta.ca.