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Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
Download from doi.orgHistorical and More Common Nongenetic Movement Disorders From Asia
Download from doi.orgGenetic Movement Disorders Commonly Seen in Asians
UploadEye‐of‐Tiger Sign in Globus Pallidus: A Novel Radiological Feature of Spinocerebellar Ataxia Type 28
Download from onlinelibrary.wiley.comMitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy
Download from academic.oup.comNovel Phenotype of 6p25 Deletion Syndrome Presenting Juvenile Parkinsonism and Brain Calcification
Download from api.wiley.comUQCRC1 Engages Cytochrome C for Neuronal Apoptotic Cell Death
Download from doi.orgHeterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population
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