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

Authors

Keywords

Myoclonus, Dystonia, Child neurology, KCTD17

Journal

Volume -, Issue -, Pages -

Publisher

Elsevier BV

Online

2018-12-07

DOI

10.1016/j.parkreldis.2018.12.001

Contact the author

Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.

Upload Now

Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.

Create Now