A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome (2018)
Source: Journal of neurology. Unidade: FM
Subjects: MIASTENIA GRAVIS, MUTAÇÃO GENÉTICA, SINAIS E SINTOMAS, BRASIL
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ABNT
ESTEPHAN, Eduardo de Paula et al. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology, v. 265, n. 3, p. 708-713, 2018Tradução . . Disponível em: https://doi.org/10.1007/s00415-018-8736-8. Acesso em: 11 ago. 2024.APA
Estephan, E. de P., Marchiori, P. E., Reed, U. C., & Zanoteli, E. (2018). A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology, 265( 3), 708-713. doi:10.1007/s00415-018-8736-8NLM
Estephan E de P, Marchiori PE, Reed UC, Zanoteli E. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome [Internet]. Journal of neurology. 2018 ; 265( 3): 708-713.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1007/s00415-018-8736-8Vancouver
Estephan E de P, Marchiori PE, Reed UC, Zanoteli E. A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome [Internet]. Journal of neurology. 2018 ; 265( 3): 708-713.[citado 2024 ago. 11 ] Available from: https://doi.org/10.1007/s00415-018-8736-8
