Source: Neuromuscular disorders. Unidade: FM
Subjects: DOENÇAS DA JUNÇÃO NEUROMUSCULAR, RECEPTORES DE ACETILCOLINA, ESTUDOS DE COORTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 09 out. 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 out. 09 ] 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 out. 09 ] Available from: https://doi.org/10.1016/j.nmd.2018.08.007