A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder

Federica Graziola; Fabrizia Stregapede; Lorena Travaglini; Giacomo Garone; Margherita Verardo; Luca Bosco; Stefano Pro; Enrico Bertini; Paolo Curatolo; Federico Vigevano; Alessandro Capuano

doi:10.1016/j.parkreldis.2018.12.001

A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder

Federica Graziola, Fabrizia Stregapede, Lorena Travaglini, Giacomo Garone, Margherita Verardo, Luca Bosco, Stefano Pro, Enrico Bertini, Paolo Curatolo, Federico Vigevano, Alessandro Capuano

Ospedale Pediatrico Bambino Gesu

Research output: Contribution to journal › Article › peer-review

Original language	English
Number of pages	3
Journal	Parkinsonism and Related Disorders
DOIs	https://doi.org/10.1016/j.parkreldis.2018.12.001
Publication status	E-pub ahead of print - Dec 7 2018

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10.1016/j.parkreldis.2018.12.001

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A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder. / Graziola, Federica; Stregapede, Fabrizia; Travaglini, Lorena; Garone, Giacomo; Verardo, Margherita; Bosco, Luca; Pro, Stefano; Bertini, Enrico; Curatolo, Paolo; Vigevano, Federico ; Capuano, Alessandro.

In: Parkinsonism and Related Disorders, 07.12.2018.

Research output: Contribution to journal › Article › peer-review

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author = "Federica Graziola and Fabrizia Stregapede and Lorena Travaglini and Giacomo Garone and Margherita Verardo and Luca Bosco and Stefano Pro and Enrico Bertini and Paolo Curatolo and Federico Vigevano and Alessandro Capuano",

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AU - Graziola, Federica

AU - Stregapede, Fabrizia

AU - Travaglini, Lorena

AU - Garone, Giacomo

AU - Verardo, Margherita

AU - Bosco, Luca

AU - Pro, Stefano

AU - Bertini, Enrico

AU - Curatolo, Paolo

AU - Vigevano, Federico

AU - Capuano, Alessandro

PY - 2018/12/7

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DO - 10.1016/j.parkreldis.2018.12.001

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JO - Parkinsonism and Related Disorders

JF - Parkinsonism and Related Disorders

SN - 1353-8020

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