Source: Muscle & Nerve. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, FENÓTIPOS, MUTAÇÃO GENÉTICA
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GURGEL-GIANNETTI, Juliana et al. Thomsen or Becker myotonia?: a novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype. Muscle & Nerve, v. 45, n. 2, p. 279-283, 2012Tradução . . Disponível em: https://doi.org/10.1002/mus.22252. Acesso em: 08 out. 2024.APA
Gurgel-Giannetti, J., Senkevics, A. S., Zilbersztajn-Gotlieb, D., Yamamoto, L. U., Muniz, V. P., Pavanello, R. C. M., et al. (2012). Thomsen or Becker myotonia?: a novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype. Muscle & Nerve, 45( 2), 279-283. doi:10.1002/mus.22252NLM
Gurgel-Giannetti J, Senkevics AS, Zilbersztajn-Gotlieb D, Yamamoto LU, Muniz VP, Pavanello RCM, Oliveira AB, Zatz M, Vainzof M. Thomsen or Becker myotonia?: a novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype [Internet]. Muscle & Nerve. 2012 ; 45( 2): 279-283.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/mus.22252Vancouver
Gurgel-Giannetti J, Senkevics AS, Zilbersztajn-Gotlieb D, Yamamoto LU, Muniz VP, Pavanello RCM, Oliveira AB, Zatz M, Vainzof M. Thomsen or Becker myotonia?: a novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype [Internet]. Muscle & Nerve. 2012 ; 45( 2): 279-283.[citado 2024 out. 08 ] Available from: https://doi.org/10.1002/mus.22252