Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients (2006)
- Authors:
- USP affiliated authors: OTTO, PAULO ALBERTO - IB ; NETTO, REGINA CELIA MINGRONI - IB
- Unidade: IB
- Subjects: DNA MITOCONDRIAL; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirão Preto
- Date published: 2006
- Source:
- Título: Brazilian Journal of Medical and Biological Research
- ISSN: 0100-879X
- Volume/Número/Paginação/Ano: v. 39, n. 2, p. 219-226, 2006
-
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: 21 fev. 2026. -
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.pdf -
NLM
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 2026 fev. 21 ] Available from: http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf -
Vancouver
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 2026 fev. 21 ] Available from: http://www.scielo.br/pdf/bjmbr/v39n2/v39n2a08.pdf - Waardenburg Syndrome: description of two novel mutations in the PAX3 gene, one of which incompletely penetrant
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