(Q47911482)
Statements
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A hereditary disorder with dementia, spastic dysarthria, vertical eye movement paresis, gait disturbance, splenomegaly, and abnormal copper metabolism. (English)
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Willvonseder R
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Goldstein NP
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McCall JT
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Yoss RE
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Tauxe WN
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1 October 1973
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23
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10
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1039-1049
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Identifiers
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