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Issue Date | Title | Author(s) |
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2014 | c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family | DANTAS, Vitor G. L.; LEZIROVITZ, Karina; YAMAMOTO, Guilherme L.; SOUZA, Carolina Fischinger Moura de; FERREIRA, Simone Gomes; MINGRONI-NETTO, Regina C. |
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