(Q43168798)
Statements
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Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation (English)
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M M Trudeau
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J C Dalton
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J W Day
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L P W Ranum
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M H Meisler
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19 October 2005
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43
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527-530
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Identifiers
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