(Q51926057)
Statements
Delineation of the clinical phenotype associated with OPHN1 mutations based on the clinical and neuropsychological evaluation of three families. (English)
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B Chabrol
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N Girard
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K N'Guyen
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A Gérard
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M Carlier
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Nicole Philip
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1 November 2005
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138
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4
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314-317
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Identifiers
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