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High Prevalence of the Connexin 26 (GJB2) Mutation in Chinese Cochlear Implant Recipients
Journal for Oto-Rhino-Laryngology, 08/26/09
Chen D et al. – The 235delC mutation was the most prevalent mutation, found in 18.3% of all cochlear implant recipients and 21.0% of the non–syndromic deafness group. Only 0.6% of GJB2 mutations were detected in the inner ear malformation group. The novel 187GT mutations are likely to be pathological mutations.
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