Response to Mortimer et al. "Clinical and molecular profiling in GNAO1 permits phenotype-genotype correlation"

Affiliations

• ¹ Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital, Barcelona, Spain.
• ² Pediatric Neurology Research Group, Vall d'Hebron Research Institute (VHIR), Autonomous University of Barcelona, Barcelona, Spain.
• ³ Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Autonomous University of Barcelona, Barcelona, Spain.
• ⁴ Department of Pediatrics, Faculty of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain.
• ⁵ European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA, Tübingen, Germany.
• ⁶ Translational Research Centre in Oncohaematology, Department of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
• ⁷ School of Medicine and Life Sciences, Far Eastern Federal University, Vladivostok, Russia.
• ⁸ Department of Pediatric Neurology, Vall Hebron University Hospital Barcelona, Barcelona, Spain.
• ⁹ European Reference Network-Rare Neurological Diseases (ERN-RND), Tübingen, Germany.
• ¹⁰ CIBER of Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.