Dantas, Vitor G. L; Raval, Dantas1, Manmeet H; Ballesteros, Angela; Cui, Runjia; Gunther, Laura K; Yamamoto, Guilherme L; Alves, Leandro Ucela; Bueno, André Silva; Lezirovitz, Karina; Pirana, Sulene; Mendes, Beatriz C. A; Yengo, Christopher M; Kachar, Bechara; Mingroni Netto, Regina Celia 
Source: Scientific Reports. Unidade: IB
Subjects: PERDA AUDITIVA, MUTAÇÃO GENÉTICA, GENÉTICA MÉDICA, GENÉTICA MOLECULAR, GENOMAS
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DANTAS, Vitor G. L et al. Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. Scientific Reports, v. 8, p. 1-15, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-26818-2. Acesso em: 06 nov. 2024.APA
Dantas, V. G. L., Raval, D. 1, Ballesteros, A., Cui, R., Gunther, L. K., Yamamoto, G. L., et al. (2018). Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss. Scientific Reports, 8, 1-15. doi:10.1038/s41598-018-26818-2NLM
Dantas VGL, Raval D1, Ballesteros A, Cui R, Gunther LK, Yamamoto GL, Alves LU, Bueno AS, Lezirovitz K, Pirana S, Mendes BCA, Yengo CM, Kachar B, Mingroni Netto RC. Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss [Internet]. Scientific Reports. 2018 ; 8 1-15.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1038/s41598-018-26818-2Vancouver
Dantas VGL, Raval D1, Ballesteros A, Cui R, Gunther LK, Yamamoto GL, Alves LU, Bueno AS, Lezirovitz K, Pirana S, Mendes BCA, Yengo CM, Kachar B, Mingroni Netto RC. Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss [Internet]. Scientific Reports. 2018 ; 8 1-15.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1038/s41598-018-26818-2
