Early-onset Parkinson's disease with atypical molecular imaging abnormalities in a patient carrying the de novo PRKCG mutation
Author:
Funder
Science and Technology Department of Zhejiang Province
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference5 articles.
1. Parkinsonism in spinocerebellar ataxia;Park;BioMed Res. Int.,2015
2. Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14;Chelban;Mov. Disord.,2018
3. Differences in MDS-UPDRS scores based on hoehn and yahr stage and disease duration;Skorvanek;Mov Disord Clin Pract,2017
4. DAT SPECT may have diagnostic value in prodromal SCA2 patients with parkinsonism;Miyaue;Park. Relat. Disord.,2017
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1. Novel mutation in exon11 of PRKCG (SCA14): A case report;Frontiers in Genetics;2023-03-08
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