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Implantation of Osmotic Pumps and Induction of Stress to Establish a Symptomatic, Pharmacological Mouse Model for DYT/PARK-ATP1A3 Dystonia
Published on: September 12, 2020
Clinical features and genetic analysis of SGCE myoclonus-dystonia: A case report
Qing Wu1, Yangyang Jiang1, Jianjun Lu1
1Department of Neurosurgery, Guangdong Second Provincial General Hospital, Guangzhou, China.
Abstract:
Myoclonus-dystonia caused by mutations in the SGCE gene is clinically characterized by early onset, myoclonus, and dystonia. Here we describe a family in which several members exhibit varying degrees of myoclonus and dystonia, caused by a novel heterozygous mutation in the SGCE gene.
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