Source: Pediatric Neurology. Unidade: FM
Subjects: DOENÇAS CONGÊNITAS, MUTAÇÃO GÊNICA, ESTUDOS DE COORTES, MIOPATIA, REVISÃO SISTEMÁTICA
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MORENO, Cristiane Araujo 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: 22 jan. 2026.APA
Moreno, C. A. M., Abath Neto, O. L., Donkervoort, S., Reed, U. C., Oliveira, A. S. B., Bönnemann, C. G., & 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 CAM, Abath Neto OL, Donkervoort S, Reed UC, Oliveira ASB, Bönnemann CG, 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 2026 jan. 22 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2017.04.002Vancouver
Moreno CAM, Abath Neto OL, Donkervoort S, Reed UC, Oliveira ASB, Bönnemann CG, 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 2026 jan. 22 ] Available from: https://doi.org/10.1016/j.pediatrneurol.2017.04.002
