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Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy (1995)

  • Authors:
  • Autor USP: AKIYAMA, JEANNE YUKIE - FM
  • Unidade: FM
  • DOI: 10.1093/hmg/4.7.1163
  • Assunto: NEUROLOGIA
  • Language: Inglês
  • Imprenta:
  • Source:
  • Acesso à fonteDOI
    Informações sobre o DOI: 10.1093/hmg/4.7.1163 (Fonte: oaDOI API)
    • Este periódico é de acesso aberto
    • Este artigo NÃO é de acesso aberto

    How to cite
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    • ABNT

      PASSOS-BUENO, Maria Rita et al. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy. Human Molecular Genetics, v. 4 , n. 7 , p. 1163-7, 1995Tradução . . Disponível em: https://doi.org/10.1093/hmg/4.7.1163. Acesso em: 14 fev. 2026.
    • APA

      Passos-Bueno, M. R., Moreira, E. S., Vainzof, M., Chamberlain, J., Marie, S. K. N., Pereira, L., et al. (1995). Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy. Human Molecular Genetics, 4 ( 7 ), 1163-7. doi:10.1093/hmg/4.7.1163
    • NLM

      Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akujama JY, Roberds S, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1093/hmg/4.7.1163
    • Vancouver

      Passos-Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SKN, Pereira L, Akujama JY, Roberds S, Campbell KP, Zatz M. Common missense mutation in the adhalin gene in three unrelated brazilian families with a relatively mild form of autosomal recessive limb girdle muscular dystrophy [Internet]. Human Molecular Genetics. 1995 ;4 ( 7 ): 1163-7.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1093/hmg/4.7.1163


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