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Genetic analysis of IRF2BPL in a Taiwanese dystonia cohort: The genotype and phenotype correlation
Introduction Dystonia is a clinically and genetically diverse movement disorder marked by sustained or intermittent muscle contractions, resulting in abnormal, frequently repetitive movements or postures.
Blood neurofilament light chain as a surrogate marker for dystonia
ORIGINAL ARTICLE This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as doi:10.1111/ene.15972. Abstract Background Dystonia is a heterogeneous movement disorder and whether neurodegeneration is involved remains inconsistent.
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