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OTOLOGY
Genotype – phenotype correlations’ limits in neurosensoral hearing loss: Case report of a three-year-old child associating a bilateral cochleovestibular impairment and a molecular variant of the COCH gene
Authors : Montava M, Roman S, Sigaudy S, Marlin S, Nicollas R, Triglia J-M. (Marseille)
Ref. : Rev Laryngol Otol Rhinol. 2012;133,3:151-156.
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