(Q50502976)
Statements
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma. (English)
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G Richard
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L E Smith
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R A Bailey
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J G Compton
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D L Paul
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S J Bale
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1 October 1998
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103
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4
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393-399
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Identifiers
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