A novel stop codon mutation in the PMP22 gene associated with a variable phenotype (2004)
Source: Neuromuscular Disorders. Unidades: IB, FM
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, ELETROFISIOLOGIA
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: 20 ago. 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.2004.01.007NLM
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 ago. 20 ] Available from: https://doi.org/10.1016/j.nmd.2004.01.007Vancouver
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 ago. 20 ] Available from: https://doi.org/10.1016/j.nmd.2004.01.007