(Q43209503)
Statements
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Vohwinkel Syndrome secondary to missense mutation D66H in GJB2 gene (connexin 26) can include epileptic manifestations (English)
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Pedro J Serrano Castro
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Cristina Naranjo Fernandez
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Pablo Quiroga Subirana
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Manuel Payan Ortiz
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19 January 2010
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19
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2
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129-131
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Identifiers
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