Source: Brazilian Journal of Medical and Biological Research. Unidade: IB
Subjects: DNA MITOCONDRIAL, MUTAÇÃO GENÉTICA
ABNT
ABREU-SILVA, Ronaldo Serafim et al. Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients. Brazilian Journal of Medical and Biological Research, v. 39, n. 2, p. 219-226, 2006Tradução . . Disponível em: http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf. Acesso em: 14 maio 2024.APA
Abreu-Silva, R. S., Lezirovitz, K., Braga, M. C. C., Spinelli, M., Pirana, S., Della-Rosa, V. A., et al. (2006). Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients. Brazilian Journal of Medical and Biological Research, 39( 2), 219-226. Recuperado de http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdfNLM
Abreu-Silva RS, Lezirovitz K, Braga MCC, Spinelli M, Pirana S, Della-Rosa VA, Otto PA, Mingroni Netto RC. Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 2): 219-226.[citado 2024 maio 14 ] Available from: http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdfVancouver
Abreu-Silva RS, Lezirovitz K, Braga MCC, Spinelli M, Pirana S, Della-Rosa VA, Otto PA, Mingroni Netto RC. Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients [Internet]. Brazilian Journal of Medical and Biological Research. 2006 ; 39( 2): 219-226.[citado 2024 maio 14 ] Available from: http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf