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X-Linked Dystonia Parkinsonism: Clinical Phenotype, Genetics and Therapeutics
Raymond L. Rosales
JMD. 2010;3(2):32-38.     DOI: https://doi.org/10.14802/jmd.10009

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X-Linked Dystonia Parkinsonism: Clinical Phenotype, Genetics and Therapeutics
Journal of Movement Disorders. 2010;3(2):32-38   Crossref logo
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Clinicopathological Phenotype and Genetics of X-Linked Dystonia–Parkinsonism (XDP; DYT3; Lubag)
Brain Sciences. 2017;7(12):72   Crossref logo
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An integrated OMICS approach unravels the elusive genetic cause of X-linked dystonia-parkinsonism
Movement Disorders. 2018;33(7):1095-1095   Crossref logo
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X-linked dystonia (“Lubag”) presenting predominantly with parkinsonism: A more benign phenotype?
Movement Disorders. 2001;17(1):200-202   Crossref logo
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A specific subtype of Infantile Parkinsonism-dystonia identified
Clinical Genetics. 2011;79(4):332-334   Crossref logo
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DYT3, X-linked Dystonia-parkinsonism (Lubag)
Encyclopedia of Movement Disorders. 2010;408-412   Crossref logo
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Eye movement deficits in X-linked dystonia-parkinsonism are related to striatal degeneration
Parkinsonism & Related Disorders. 2019;61:170-178   Crossref logo
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Increased insula-putamen connectivity in X-linked dystonia-parkinsonism
NeuroImage: Clinical. 2018;17:835-846   Crossref logo
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Genetics in dystonia
Parkinsonism & Related Disorders. 2014;20:S137-S142   Crossref logo
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ATP1A3 mutation presenting as CAPOS syndrome + dystonia phenotype
Parkinsonism & Related Disorders. 2020;78:192-194   Crossref logo
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