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Mov Disord 2008 Dec 31.
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A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype-phenotype correlations. [JOURNAL ARTICLE]
Mov Disord 2008 Dec 31.
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Huntington disease in subjects from an Israeli Karaite community carrying alleles of intermediate and expanded CAG repeats in the HTT gene: Huntington disease or phenocopy? [JOURNAL ARTICLE]
J Neurol Sci 2008 Dec 5.
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Movement disorder emergencies. [Journal Article]
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Weight loss in Huntington disease increases with higher CAG repeat number. [Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't]
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Paroxysmal Non-Kinesigenic Dyskinesia Caused by the Mutation of MR-1 in a Large Polish Kindred. [JOURNAL ARTICLE]
Eur Neurol 2008 Oct 24; 61(1):39-41.
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No evidence of perfusion abnormalities in the basal ganglia of a patient with generalized chorea-ballism and polycythaemia vera: analysis using subtraction SPECT co-registered to MRI. [Journal Article]
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Huntingtin modulates transcription, occupies gene promoters in vivo, and binds directly to DNA in a polyglutamine-dependent manner. [Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
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