A novel stop codon mutation in the PMP22 gene associated with a variable phenotype (2002)
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS
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ABE, Kikue Terada et al. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 20 ago. 2024. , 2002APA
Abe, K. T., Passos-Bueno, M. R., Pavanello, R. de C. M., Lino, A. M. M., Hirata, M. T. A., Brotto, M. W., et al. (2002). A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. Oxford: Instituto de Biociências, Universidade de São Paulo.NLM
Abe KT, Passos-Bueno MR, Pavanello R de CM, Lino AMM, Hirata MTA, Brotto MW, Marchiori PE, Zatz M. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. 2002 ; 12( 7-8): 762-763.[citado 2024 ago. 20 ]Vancouver
Abe KT, Passos-Bueno MR, Pavanello R de CM, Lino AMM, Hirata MTA, Brotto MW, Marchiori PE, Zatz M. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders. 2002 ; 12( 7-8): 762-763.[citado 2024 ago. 20 ]