A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder. (April 2019)
- Record Type:
- Journal Article
- Title:
- A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder. (April 2019)
- Main Title:
- A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder
- Authors:
- Graziola, Federica
Stregapede, Fabrizia
Travaglini, Lorena
Garone, Giacomo
Verardo, Margherita
Bosco, Luca
Pro, Stefano
Bertini, Enrico
Curatolo, Paolo
Vigevano, Federico
Capuano, Alessandro - Abstract:
- Is Part Of:
- Parkinsonism & related disorders. Volume 61(2019)
- Journal:
- Parkinsonism & related disorders
- Issue:
- Volume 61(2019)
- Issue Display:
- Volume 61, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 61
- Issue:
- 2019
- Issue Sort Value:
- 2019-0061-2019-0000
- Page Start:
- 4
- Page End:
- 6
- Publication Date:
- 2019-04
- Subjects:
- Myoclonus -- Dystonia -- Child neurology -- KCTD17
Parkinson's disease -- Periodicals
Movement disorders -- Periodicals
Movement Disorders -- Periodicals
Nerve Degeneration -- Periodicals
Nervous System Diseases -- Periodicals
Parkinson Disease -- Periodicals
Tremor -- Periodicals
Parkinson, Maladie de -- Périodiques
Parkinson's disease
616.833 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13538020 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/13538020 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/13538020 ↗
http://www.prd-journal.com/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.parkreldis.2018.12.001 ↗
- Languages:
- English
- ISSNs:
- 1353-8020
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6406.787000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23145.xml