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A de novo loss-of-function DYNC1H1 mutation in a patient with parkinsonian features and a favourable response to
K Szczałuba1, K Szymańska2, M Rydzanicz1
1Department of Medical Genetics, Medical University of Warsaw, Warsaw, Poland.
Clinical Genetics
|December 16, 2017
Abstract:
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..
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