Source: BMC Medical Genetics. Unidade: IB
Subjects: SURDEZ, HEREDITARIEDADE, MUTAÇÃO GENÉTICA, PERDA AUDITIVA BILATERAL, PACIENTES
ABNT
NONOSE, Renata Watanabe et al. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects. BMC Medical Genetics, v. 19, p. 1-10, 2018Tradução . . Disponível em: https://doi.org/10.1186/s12881-018-0585-x. Acesso em: 06 nov. 2024.APA
Nonose, R. W., Lezirovitz, K., Auricchio, M. T. B. D. M., Batissoco, A. C., Yamamoto, G. L., & Mingroni Netto, R. C. (2018). Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects. BMC Medical Genetics, 19, 1-10. doi:10.1186/s12881-018-0585-xNLM
Nonose RW, Lezirovitz K, Auricchio MTBDM, Batissoco AC, Yamamoto GL, Mingroni Netto RC. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects [Internet]. BMC Medical Genetics. 2018 ; 19 1-10.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/s12881-018-0585-xVancouver
Nonose RW, Lezirovitz K, Auricchio MTBDM, Batissoco AC, Yamamoto GL, Mingroni Netto RC. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing- impaired subjects [Internet]. BMC Medical Genetics. 2018 ; 19 1-10.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1186/s12881-018-0585-x