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OBJECTIVE Hereditary nonsyndromic deafness is an autosomal recessive condition in about 80% of cases, and point mutations in the GJB2 gene (connexin 26) and two deletions in the GJB6 gene (connexin(More)
Instituição: Otolaryngology Department, University of São Paulo Medical School, São Paulo, Brazil / Institute of Biosciences, University of São Paulo, São Paulo, Brazil Endereço para correspondência:(More)