Source: American Journal of Human Genetics. Unidade: FM
Subjects: DISTROFIA MUSCULAR, FENÓTIPOS, DELEÇÃO DE GENES, MUTAÇÃO GENÉTICA
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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: 18 nov. 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 nov. 18 ]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 nov. 18 ]
