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See Latest ArticlesGJB2 and GJB6 Genes: Molecular Study and Identification of Novel GJB2 Mutations in the Hearing-Impaired Argentinean Population
Audiology & Neuro-Otology, 11/04/09
Dalamon V et al. – This work shows the high prevalence of GJB2 mutations in the Argentinean population, with frequencies that are comparable to those of the Mediterranean area. Most important, it adds two novel GJB2 mutations to be taken into consideration in the genetic diagnosis of non–syndromic sensorineural hearing loss.
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