(Q48858209)
Statements
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Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness (English)
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R Bruzzone
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D Gomès
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E Denoyelle
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N Duval
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J Perea
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V Veronesi
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D Weil
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M M Gabellec
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P D'Andrea
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T W White
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1 January 2001
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8
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4-6
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425-431
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Identifiers
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