Source: Pediatric Neurology. Unidade: FM
Subjects: DOENÇAS CONGÊNITAS, MUTAÇÃO GÊNICA, ESTUDOS DE COORTES, MIOPATIA, REVISÃO SISTEMÁTICA
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MORENO, Cristiane de Araújo Martins et al. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature. Pediatric Neurology, v. 75, p. 11-16, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.pediatrneurol.2017.04.002. Acesso em: 16 out. 2024.APA
Moreno, C. de A. M., Abath Neto, O., Donkervoort, S., Reed, U. C., Oliveira, A. S. B., Bönnemann, C., & Zanoteli, E. (2017). Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature. Pediatric Neurology, 75, 11-16. doi:10.1016/j.pediatrneurol.2017.04.002NLM
Moreno C de AM, Abath Neto O, Donkervoort S, Reed UC, Oliveira ASB, Bönnemann C, Zanoteli E. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature [Internet]. Pediatric Neurology. 2017 ; 75 11-16.[citado 2024 out. 16 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2017.04.002Vancouver
Moreno C de AM, Abath Neto O, Donkervoort S, Reed UC, Oliveira ASB, Bönnemann C, Zanoteli E. Clinical and Histologic Findings in ACTA1-Related Nemaline Myopathy: Case Series and Review of the Literature [Internet]. Pediatric Neurology. 2017 ; 75 11-16.[citado 2024 out. 16 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2017.04.002