Source: Neuromuscular disorders. Unidade: FM
Subjects: DOENÇAS DA JUNÇÃO NEUROMUSCULAR, RECEPTORES DE ACETILCOLINA, ESTUDOS DE COORTES
ABNT
ESTEPHAN, Eduardo de Paula et al. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil. Neuromuscular disorders, v. 28, n. 11, p. 961-964, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2018.08.007. Acesso em: 29 maio 2024.APA
Estephan, E. de P., Zambon, A. A., Marchiori, P. E., Silva, A. M. S. da, Caldas, V. M., Moreno, C. A. M., et al. (2018). Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil. Neuromuscular disorders, 28( 11), 961-964. doi:10.1016/j.nmd.2018.08.007NLM
Estephan E de P, Zambon AA, Marchiori PE, Silva AMS da, Caldas VM, Moreno CAM, Reed UC, Horvath R, Topf A, Lochmueller H. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil [Internet]. Neuromuscular disorders. 2018 ; 28( 11): 961-964.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.nmd.2018.08.007Vancouver
Estephan E de P, Zambon AA, Marchiori PE, Silva AMS da, Caldas VM, Moreno CAM, Reed UC, Horvath R, Topf A, Lochmueller H. Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in Brazil [Internet]. Neuromuscular disorders. 2018 ; 28( 11): 961-964.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.nmd.2018.08.007