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; LINO, A. M. M.; HIRATA, M. T. A.; et al. A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. Neuromuscular Disorders, Amsterdam, v. 14, n. 5, p. 313-320, 2004. Disponível em: < http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6T9T-4C0TCXK-1-5&_cdi=5123&_orig=browse&_coverDate=05%2F31%2F2004&_sk=999859994&view=c&wchp=dGLbVzz-zSkWz&_acct=C000049650&_version=1&_userid=972067&md5=6b98ce09811227f352c > DOI: 10.1016/j.nmd.2004.01.007.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.Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6T9T-4C0TCXK-1-5&_cdi=5123&_orig=browse&_coverDate=05%2F31%2F2004&_sk=999859994&view=c&wchp=dGLbVzz-zSkWz&_acct=C000049650&_version=1&_userid=972067&md5=6b98ce09811227f352cVancouver
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.Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6T9T-4C0TCXK-1-5&_cdi=5123&_orig=browse&_coverDate=05%2F31%2F2004&_sk=999859994&view=c&wchp=dGLbVzz-zSkWz&_acct=C000049650&_version=1&_userid=972067&md5=6b98ce09811227f352c