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Filtros : "Ferreiro-Barros, Claudia C." Limpar

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  • Artigo de periodico

    Mitochondrial translation in health and disease (2013)

    Ferreiro-Barros, Claudia C.; Barros, Mário Henrique de

    Source: Open Journal of Endocrine and Metabolic Diseases. Unidade: ICB

    Assunto: MICROBIOLOGIA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      FERREIRO-BARROS, Claudia C. e BARROS, Mário Henrique de. Mitochondrial translation in health and disease. Open Journal of Endocrine and Metabolic Diseases, v. 3, p. 1-9, 2013Tradução . . Disponível em: https://doi.org/10.4236/ojemd.2013.32A001. Acesso em: 29 maio 2024.

    • APA

      Ferreiro-Barros, C. C., & Barros, M. H. de. (2013). Mitochondrial translation in health and disease. Open Journal of Endocrine and Metabolic Diseases, 3, 1-9. doi:10.4236/ojemd.2013.32A001

    • NLM

      Ferreiro-Barros CC, Barros MH de. Mitochondrial translation in health and disease [Internet]. Open Journal of Endocrine and Metabolic Diseases. 2013 ;3 1-9.[citado 2024 maio 29 ] Available from: https://doi.org/10.4236/ojemd.2013.32A001

    • Vancouver

      Ferreiro-Barros CC, Barros MH de. Mitochondrial translation in health and disease [Internet]. Open Journal of Endocrine and Metabolic Diseases. 2013 ;3 1-9.[citado 2024 maio 29 ] Available from: https://doi.org/10.4236/ojemd.2013.32A001

  • Artigo de periodico

    Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation (2012)

    Garcia-Diaz, Beatriz; Barros, Mário Henrique de ; Sanna-Cherchi, Simone; Emmanuele, Valentina; Akman, Hasan O.; Ferreiro-Barros, Claudia C.; Horvath, Rita; Tadesse, Saba; El Gharaby, Nader; Di Mauro, Salvatore; De Vivo, Darryl C.; Shokr, Aly; Hirano, Michio; Quinzii, Catarina M.

    Source: American Journal of Human Genetics. Unidade: ICB

    Assunto: MICROBIOLOGIA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      GARCIA-DIAZ, Beatriz et al. Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation. American Journal of Human Genetics, v. 91, n. 4, p. 729-736, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2012.08.019. Acesso em: 29 maio 2024.

    • APA

      Garcia-Diaz, B., Barros, M. H. de, Sanna-Cherchi, S., Emmanuele, V., Akman, H. O., Ferreiro-Barros, C. C., et al. (2012). Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation. American Journal of Human Genetics, 91( 4), 729-736. doi:10.1016/j.ajhg.2012.08.019

    • NLM

      Garcia-Diaz B, Barros MH de, Sanna-Cherchi S, Emmanuele V, Akman HO, Ferreiro-Barros CC, Horvath R, Tadesse S, El Gharaby N, Di Mauro S, De Vivo DC, Shokr A, Hirano M, Quinzii CM. Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation [Internet]. American Journal of Human Genetics. 2012 ; 91( 4): 729-736.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.ajhg.2012.08.019

    • Vancouver

      Garcia-Diaz B, Barros MH de, Sanna-Cherchi S, Emmanuele V, Akman HO, Ferreiro-Barros CC, Horvath R, Tadesse S, El Gharaby N, Di Mauro S, De Vivo DC, Shokr A, Hirano M, Quinzii CM. Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation [Internet]. American Journal of Human Genetics. 2012 ; 91( 4): 729-736.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.ajhg.2012.08.019
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