Dantas, Vitor G. L.; Lezirovitz, Karina; Yamamoto, Guilherme L; Souza, Carolina Fischinger Moura de; Ferreira, Simone Gomes; Mingroni Netto, Regina Celia 
Source: Genetics and Molecular Biology. Unidade: IB
Subjects: SURDEZ, PERDA AUDITIVA DE ALTA FREQUÊNCIA, MUTAÇÃO GENÉTICA, MAPEAMENTO GENÉTICO
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DANTAS, Vitor G. L. et al. c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family. Genetics and Molecular Biology, p. on-line, 2014Tradução . . Disponível em: https://doi.org/10.1590/S1415-47572014005000025. Acesso em: 14 nov. 2024.APA
Dantas, V. G. L., Lezirovitz, K., Yamamoto, G. L., Souza, C. F. M. de, Ferreira, S. G., & Mingroni Netto, R. C. (2014). c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family. Genetics and Molecular Biology, on-line. doi:10.1590/S1415-47572014005000025NLM
Dantas VGL, Lezirovitz K, Yamamoto GL, Souza CFM de, Ferreira SG, Mingroni Netto RC. c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family [Internet]. Genetics and Molecular Biology. 2014 ; on-line.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1590/S1415-47572014005000025Vancouver
Dantas VGL, Lezirovitz K, Yamamoto GL, Souza CFM de, Ferreira SG, Mingroni Netto RC. c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family [Internet]. Genetics and Molecular Biology. 2014 ; on-line.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1590/S1415-47572014005000025
