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Filtros : "Pan, Te-Cheng" Limpar

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  • Artigo de periodico

    Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT (2010)

    Zhang, Rui-Zhu; Zou, Yaqun; Pan, Te-Cheng; Markova, Dessislava; Fertala, Andrzej; Hu, Ying; Squarzoni, Stefano; Reed, Umbertina Conti; Marie, Suely K. N.; Bönnemann, Carsten G.; Chu, Mon-Li

    Source: Journal of Biological Chemistry. Unidade: FM

    Subjects: NUCLEOTÍDEOS, LIPOSSOMOS, ENZIMAS

    Acesso à fonteHow to cite
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    • ABNT

      ZHANG, Rui-Zhu et al. Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT. Journal of Biological Chemistry, v. 285, n. 13, p. 10005-10015, 2010Tradução . . Disponível em: http://www.jbc.org/content/285/13/10005.full.pdf+html?sid=eeab1c98-270a-4290-aab5-a14a91331c4f. Acesso em: 05 out. 2024.

    • APA

      Zhang, R. -Z., Zou, Y., Pan, T. -C., Markova, D., Fertala, A., Hu, Y., et al. (2010). Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT. Journal of Biological Chemistry, 285( 13), 10005-10015. Recuperado de http://www.jbc.org/content/285/13/10005.full.pdf+html?sid=eeab1c98-270a-4290-aab5-a14a91331c4f

    • NLM

      Zhang R-Z, Zou Y, Pan T-C, Markova D, Fertala A, Hu Y, Squarzoni S, Reed UC, Marie SKN, Bönnemann CG, Chu M-L. Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT [Internet]. Journal of Biological Chemistry. 2010 ; 285( 13): 10005-10015.[citado 2024 out. 05 ] Available from: http://www.jbc.org/content/285/13/10005.full.pdf+html?sid=eeab1c98-270a-4290-aab5-a14a91331c4f

    • Vancouver

      Zhang R-Z, Zou Y, Pan T-C, Markova D, Fertala A, Hu Y, Squarzoni S, Reed UC, Marie SKN, Bönnemann CG, Chu M-L. Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT [Internet]. Journal of Biological Chemistry. 2010 ; 285( 13): 10005-10015.[citado 2024 out. 05 ] Available from: http://www.jbc.org/content/285/13/10005.full.pdf+html?sid=eeab1c98-270a-4290-aab5-a14a91331c4f

  • Artigo de periodico

    New molecular mechanism for ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype (2003)

    Pan, Te-Cheng; Zhang, Rui Zhu; Sudano, Dominick G.; Marie, Suely K.; Bonnemann, Carsten G.; Chu, Mon Li

    Source: American Journal of Human Genetics. Unidade: FM

    Subjects: DISTROFIA MUSCULAR, FENÓTIPOS, DELEÇÃO DE GENES, MUTAÇÃO GENÉTICA

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

    • ABNT

      PAN, Te-Cheng et al. New molecular mechanism for ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype. American Journal of Human Genetics, v. 73, p. 355-369, 2003Tradução . . Acesso em: 05 out. 2024.

    • APA

      Pan, T. -C., Zhang, R. Z., Sudano, D. G., Marie, S. K., Bonnemann, C. G., & Chu, M. L. (2003). New molecular mechanism for ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype. American Journal of Human Genetics, 73, 355-369.

    • NLM

      Pan T-C, Zhang RZ, Sudano DG, Marie SK, Bonnemann CG, Chu ML. New molecular mechanism for ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype. American Journal of Human Genetics. 2003 ; 73 355-369.[citado 2024 out. 05 ]

    • Vancouver

      Pan T-C, Zhang RZ, Sudano DG, Marie SK, Bonnemann CG, Chu ML. New molecular mechanism for ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype. American Journal of Human Genetics. 2003 ; 73 355-369.[citado 2024 out. 05 ]
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