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Updated: Dec 14, 2025

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
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Movement disorders rounds: Atypical cases in two Chinese families with novel variants in ATP1A3
Xin-Yao Li1, Yue-Hui Hong1, Lin Wang1
1Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, 100730, China.
Parkinsonism & Related Disorders
|July 21, 2020
Abstract:
ATP1A3-related dystonia is a disorder with high heterogeneous spectrum of clinical manifestations caused by mutations in ATP1A3 gene. Here, 2 atypical cases carring 2 de-novo ATP1A3 variants with RDP-CAPOS overlapping phenotype or continuous hemi-dystonia are described.
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