Mutations inMICAL-1cause autosomal-dominant lateral temporal epilepsy

Author:

Dazzo Emanuela1,Rehberg Kati2,Michelucci Roberto3,Passarelli Daniela4,Boniver Clementina5,Vianello Dri Valeria6,Striano Pasquale7ORCID,Striano Salvatore8,Pasterkamp R. Jeroen2,Nobile Carlo19

Affiliation:

1. CNR-Neuroscience Institute; Section of Padua; Padova Italy

2. Department of Translational Neuroscience, Brain Center Rudolf Magnus; UMC Utrecht, Utrecht University; Utrecht The Netherlands

3. IRCCS-Institute of Neurological Sciences of Bologna, Unit of Neurology, Bellaria Hospital; Bologna Italy

4. Division of Neurology; Infermi Hospital; Faenza Italy

5. Clinical Neurophysiology, Department of Pediatrics; University of Padua; Padova Italy

6. APSS Trento, Mental Health Department; Child and Adolescent Neuropsichiatry 1; Trento Italy

7. Pediatric Neurology and Muscular Diseases Unit, Department of Neurosciences; Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, “G. Gaslini” Institute; Genova Italy

8. Department of Neurological Sciences; Federico II University; Napoli Italy

9. Department of Biomedical Sciences; University of Padua; Padova Italy

Funder

Telethon-Italy

The Netherlands Organization for Scientific Research

Epilepsiefonds

Fondazione Telethon

Publisher

Wiley

Subject

Clinical Neurology,Neurology

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