(Q41722886)
Statements
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Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I. (English)
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Agid Y
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Dürr A
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Brice A
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Rivaud-Pechoux S
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Gaymard B
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Cancel G
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Ploner CJ
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Pierrot-Deseilligny C
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Identifiers
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