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pubmed-article:1301515pubmed:abstractTextA family is described in which closely consanguineous parents had Huntington chorea and in their son a severe hypertonic-hypokinetic syndrome with pellagra-like cutaneous changes was present. In two generations of the family in 6 subjects involuntary movements and gait disorders were reported.lld:pubmed
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pubmed-article:1301515pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:1301515pubmed:articleTitle[Contribution to the clinical polymorphism in Huntington's disease].lld:pubmed
pubmed-article:1301515pubmed:affiliationII Katedry i Kliniki Neurologii Sl. AM, Zabrzu.lld:pubmed
pubmed-article:1301515pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1301515pubmed:publicationTypeEnglish Abstractlld:pubmed