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

• Kara Goodkey,
• Anita Wischmeijer,
• Laurence Perrin,
• Adrianne E. S. Watson,
• Leenah Qureshi,
• Duccio Maria Cordelli,
• Francesco Toni,
• Maria Gnazzo,
• Francesco Benedicenti,
• Monique Elmaleh‑Berges,
• Karen J. Low,
• Anastassia Voronova

Affiliations

Kara Goodkey

Department of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta

Anita Wischmeijer

Clinical Genetics Service and Coordination Center for Rare Diseases, Department of Pediatrics, Regional Hospital of Bolzano

Laurence Perrin

Clinical Genetics Unit, Hopital Robert-Debre

Adrianne E. S. Watson

Department of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta

Leenah Qureshi

Department of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta

Duccio Maria Cordelli

IRCCS Istituto Delle Scienze Neurologiche Di Bologna, UOC Neuropsichiatria Dell’eta Pediatrica

Francesco Toni

Programma Di Neuroradiologia Con Tecniche Ad Elevata Complessita (PNTEC), IRCCS Istituto Delle Scienze Neurologiche Di Bologna

Maria Gnazzo

Laboratory of Medical Genetics, Translational Cytogenomics Research Unit, Bambino Gesu Children’s Hospital, IRCCS

Francesco Benedicenti

Clinical Genetics Service and Coordination Center for Rare Diseases, Department of Pediatrics, Regional Hospital of Bolzano

Monique Elmaleh‑Berges

Service d’Imagerie Pediatrique, Hopital Universitaire Robert Debre

Karen J. Low

Department of Academic Child Health, Bristol Medical School, Population Health Sciences, University of Bristol

Anastassia Voronova

Department of Medical Genetics, Faculty of Medicine & Dentistry, University of Alberta