Novel SEPSECS Pathogenic Variants Featuring Unusual Phenotype of Complex Movement Disorder With Thin Corpus Callosum
A Case Report
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Article Information
- Received October 13, 2021
- Accepted in final form January 24, 2022
- First Published March 3, 2022.
Author Disclosures
- Francesco Nicita, MD, PhD,
- Lorena Travaglini, PhD (lorena.travaglini{at}opbg.net),
- Francesco Bombelli, MD (francescobombelli{at}gmail.com),
- Michele Tosi, MD (michele.tosi{at}opbg.net),
- Stefano Pro, MD (stefano.pro{at}opbg.net),
- Enrico Bertini, MD (enricosilvio.bertini{at}opbg.net) and
- Adele D'Amico, MD, PhD (adele2.damico{at}opbg.net)
- Francesco Nicita, MD, PhD,
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Associate Editor or Editorial Board Member of the following Journals: - Frontiers in Neurology - Pediatric Neurology Section - Brain Sciences - Journal of Integrative Neurosciences
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- Lorena Travaglini, PhD (lorena.travaglini{at}opbg.net),
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- Francesco Bombelli, MD (francescobombelli{at}gmail.com),
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- Michele Tosi, MD (michele.tosi{at}opbg.net),
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- Stefano Pro, MD (stefano.pro{at}opbg.net),
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- Enrico Bertini, MD (enricosilvio.bertini{at}opbg.net) and
(1) Roche advisory board; (2)Biogen advisory Board; (3) Avexis Advisory Board
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(1) Italian Ministry of Health
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- Adele D'Amico, MD, PhD (adele2.damico{at}opbg.net)
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- From the Genetics and Rare Diseases Research Division (N.D.F., L.T., M.T., E.B., A.D.A.), Unit of Neuromuscular and Neurodegenerative Disorders, Department of Neurosciences, Bambino Gesù Children's Hospital, IRCCS; Studio Neurologico Laterano (F.B.); and Neurophysiology Unit (S.P.), Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
- Correspondence
Dr. Nicita francesco.nicita{at}opbg.net
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