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Updated: Jan 31, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder
Federica Graziola1, Fabrizia Stregapede2, Lorena Travaglini3
1Department of Neuroscience, Movement Disorders Clinic, Bambino Gesù Children's Hospital, Viale San Paolo 15, 00146, Rome, Italy; Department of Neuroscience, Child Neurology and Psychiatry Unit, Tor Vergata University Hospital, Viale Oxford 81, 00133, Rome, Italy.
No abstract available in PubMed .
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