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  • Artigo de periodico

    The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry (2022)

    Ali, Taccyanna M.; Linnenkamp, Bianca D. W.; Yamamoto, Guilherme L.; Honjo, Rachel S.; Menezes Filho, Hamilton Cabral de; Kim, Chong Ae ; Bertola, Debora R.

    Source: American journal of medical genetics part a. Unidade: FM

    Subjects: FRATURAS, ANCESTRAIS, PREVALÊNCIA, FENÓTIPOS

    Acesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      ALI, Taccyanna M. et al. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry. American journal of medical genetics part a, v. 188, n. 5, p. 1545-1549, 2022Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.62651. Acesso em: 08 nov. 2025.

    • APA

      Ali, T. M., Linnenkamp, B. D. W., Yamamoto, G. L., Honjo, R. S., Menezes Filho, H. C. de, Kim, C. A., & Bertola, D. R. (2022). The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry. American journal of medical genetics part a, 188( 5), 1545-1549. doi:10.1002/ajmg.a.62651

    • NLM

      Ali TM, Linnenkamp BDW, Yamamoto GL, Honjo RS, Menezes Filho HC de, Kim CA, Bertola DR. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry [Internet]. American journal of medical genetics part a. 2022 ; 188( 5): 1545-1549.[citado 2025 nov. 08 ] Available from: https://doi.org/10.1002/ajmg.a.62651

    • Vancouver

      Ali TM, Linnenkamp BDW, Yamamoto GL, Honjo RS, Menezes Filho HC de, Kim CA, Bertola DR. The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry [Internet]. American journal of medical genetics part a. 2022 ; 188( 5): 1545-1549.[citado 2025 nov. 08 ] Available from: https://doi.org/10.1002/ajmg.a.62651

  • Artigo de periodico

    Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype (2015)

    Vieira, Natássia M; Guo, Ling T; Estrela, Elicia; Kunkel, Louis M; Zatz, Mayana ; Shelton, G. Diane

    Source: Neuromuscular Disorders. Unidade: IB

    Subjects: DISTROFIA MUSCULAR, MODELOS ANIMAIS, CÃO LABRADOR RETRIEVER, MUTAÇÃO GENÉTICA

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

    • ABNT

      VIEIRA, Natássia M et al. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype. Neuromuscular Disorders, v. 25, p. 363-370, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2015.02.012. Acesso em: 08 nov. 2025.

    • APA

      Vieira, N. M., Guo, L. T., Estrela, E., Kunkel, L. M., Zatz, M., & Shelton, G. D. (2015). Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype. Neuromuscular Disorders, 25, 363-370. doi:10.1016/j.nmd.2015.02.012

    • NLM

      Vieira NM, Guo LT, Estrela E, Kunkel LM, Zatz M, Shelton GD. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype [Internet]. Neuromuscular Disorders. 2015 ; 25 363-370.[citado 2025 nov. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.012

    • Vancouver

      Vieira NM, Guo LT, Estrela E, Kunkel LM, Zatz M, Shelton GD. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype [Internet]. Neuromuscular Disorders. 2015 ; 25 363-370.[citado 2025 nov. 08 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.012
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