A de novo loss-of-function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa.
Krzysztof SzczalubaK SzymańskaM RydzaniczElżbieta CiaraA WalczakD Piekutowska-AbramczukJ KosińskaA JacoszekK CzerskaA BiernackaM Laure-KamionowskaP GasperowiczE PronickaPloski RafalPublished in: Clinical genetics (2017)
Graphical summary of 'A de novo loss-of-function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to levodopa' by Szczałuba et al..