Lack of mutations in spinocerebellar ataxia type 2 and 3 genes in a Taiwanese (ethnic Chinese) cohort of familial and early-onset parkinsonism
Author:
Publisher
Wiley
Subject
Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)
Reference32 articles.
1. Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism
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1. A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing;Movement Disorders;2019-02-20
2. Pathophysiology of Small-Fiber Sensory System in Parkinson's Disease;Medicine;2016-03
3. Parkinsonism in Spinocerebellar Ataxia;BioMed Research International;2015
4. Mutational Analysis of Angiogenin Gene in Parkinson's Disease;PLoS ONE;2014-11-11
5. Lack of C9orf72 Repeat Expansion in Taiwanese Patients with Mixed Neurodegenerative Disorders;Frontiers in Neurology;2014-04-28
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