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Filtros : "Holanda" "Neuromuscular Disorders" Limpar

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  • Artigo de periodico

    A novel stop codon mutation in the PMP22 gene associated with a variable phenotype (2004)

    Abe, Kikue Terada; Lino, A. M. M.; Hirata, M. T. A.; Pavanello, Rita de Cássia M.; Brotto, Mário Wilson Iervolino; Marchiori, Paulo Eurípedes; Zatz, Mayana

    Source: Neuromuscular Disorders. Unidades: IB, FM

    Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, ELETROFISIOLOGIA

    Acesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      ABE, Kikue Terada et al. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders, v. 14, n. 5, p. 313-320, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2004.01.007. Acesso em: 08 out. 2024.

    • APA

      Abe, K. T., Lino, A. M. M., Hirata, M. T. A., Pavanello, R. de C. M., Brotto, M. W. I., Marchiori, P. E., & Zatz, M. (2004). A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders, 14( 5), 313-320. doi:10.1016/j.nmd.2004.01.007

    • NLM

      Abe KT, Lino AMM, Hirata MTA, Pavanello R de CM, Brotto MWI, Marchiori PE, Zatz M. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype [Internet]. Neuromuscular Disorders. 2004 ; 14( 5): 313-320.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2004.01.007

    • Vancouver

      Abe KT, Lino AMM, Hirata MTA, Pavanello R de CM, Brotto MWI, Marchiori PE, Zatz M. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype [Internet]. Neuromuscular Disorders. 2004 ; 14( 5): 313-320.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.nmd.2004.01.007

  • Artigo de periodico

    Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? (2002)

    Tonini, M. M. O.; Passos-Bueno, Maria Rita ; Cerqueira, A.; Pavanello, Rita de Cássia M.; Vainzof, Mariz ; Dubowitz, Victor; Zatz, Mayana

    Source: Neuromuscular Disorders. Unidade: IB

    Assunto: DISTROFIA MUSCULAR

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

    • ABNT

      TONINI, M. M. O. et al. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye?. Neuromuscular Disorders, v. 12, n. 6, p. 554-557, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0960-8966(02)00014-7. Acesso em: 08 out. 2024.

    • APA

      Tonini, M. M. O., Passos-Bueno, M. R., Cerqueira, A., Pavanello, R. de C. M., Vainzof, M., Dubowitz, V., & Zatz, M. (2002). Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? Neuromuscular Disorders, 12( 6), 554-557. doi:10.1016/s0960-8966(02)00014-7

    • NLM

      Tonini MMO, Passos-Bueno MR, Cerqueira A, Pavanello R de CM, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? [Internet]. Neuromuscular Disorders. 2002 ; 12( 6): 554-557.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/s0960-8966(02)00014-7

    • Vancouver

      Tonini MMO, Passos-Bueno MR, Cerqueira A, Pavanello R de CM, Vainzof M, Dubowitz V, Zatz M. Facioscapulohumeral (FSHD1) and other forms of muscular dystrophy in the same family: is there more in muscular dystrophy than meets the eye? [Internet]. Neuromuscular Disorders. 2002 ; 12( 6): 554-557.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/s0960-8966(02)00014-7
  • 1

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