Expanding the genetic and phenotypic spectrum of CHD2 ‐related disease: From early neurodevelopmental disorders to adult‐onset epilepsy

Author:

De Maria Beatrice1,Balestrini Simona12ORCID,Mei Davide1ORCID,Melani Federico1ORCID,Pellacani Simona1ORCID,Pisano Tiziana1ORCID,Rosati Anna1ORCID,Scaturro Giusi M.3,Giordano Lucio4ORCID,Cantalupo Gaetano567ORCID,Fontana Elena56,Zammarchi Cristina8,Said Edith9,Leuzzi Vincenzo10ORCID,Mastrangelo Mario10ORCID,Galosi Serena10ORCID,Parrini Elena1ORCID,Guerrini Renzo1ORCID

Affiliation:

1. Paediatric Neurology Unit and Laboratories A. Meyer Children's Hospital, University of Florence Florence Italy

2. Department of Clinical and Experimental Epilepsy UCL Queen Square Institute of Neurology, and Chalfont Centre for Epilepsy Gerrard Cross UK

3. Metabolic Diseases Unit A. Meyer Children's Hospital, University of Florence Florence Italy

4. Paediatric Neurology and Psychiatry Unit Spedali Civili Children's Hospital, University of Brescia Brescia Italy

5. Child Neuropsychiatry Section, Department of Surgical Sciences, Dentistry, Gynecology and Paediatrics University of Verona Verona Italy

6. Dipartimento Materno‐Infantile UOC Neuropsichiatria Infantile, Azienda Ospedaliero‐Universitaria Integrata Verona Italy

7. Center for Research on Epilepsies in Pediatric age (CREP) Verona Italy

8. Paediatric Neurology and Psychiatry Unit Infermi Hospital Rimini Italy

9. Section of Medical Genetics, Department of Pathology Mater Dei Hospital Msida Malta

10. Child Neurology and Psychiatry, Department of Human Neuroscience Sapienza University of Rome Rome Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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