Congenital myasthenic syndrome: correlation between clinical features and molecular diagnosis (2022)
Source: European journal of neurology. Unidade: FM
Subjects: DOENÇAS NEUROMUSCULARES, MIASTENIA GRAVIS, IMAGEM POR RESSONÂNCIA MAGNÉTICA, DIAGNÓSTICO POR IMAGEM
ABNT
ESTEPHAN, Eduardo P et al. Congenital myasthenic syndrome: correlation between clinical features and molecular diagnosis. European journal of neurology, v. 29, n. 3, p. 833-842, 2022Tradução . . Disponível em: https://doi.org/10.1111/ene.15173. Acesso em: 13 nov. 2024.APA
Estephan, E. P., Zambon, A. A., Thompson, R., Polavarapu, K., Jomaa, D., Topf, A., et al. (2022). Congenital myasthenic syndrome: correlation between clinical features and molecular diagnosis. European journal of neurology, 29( 3), 833-842. doi:10.1111/ene.15173NLM
Estephan EP, Zambon AA, Thompson R, Polavarapu K, Jomaa D, Topf A, Helito PVP, Moreno CAM, Reed UC, Zanoteli E. Congenital myasthenic syndrome: correlation between clinical features and molecular diagnosis [Internet]. European journal of neurology. 2022 ; 29( 3): 833-842.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1111/ene.15173Vancouver
Estephan EP, Zambon AA, Thompson R, Polavarapu K, Jomaa D, Topf A, Helito PVP, Moreno CAM, Reed UC, Zanoteli E. Congenital myasthenic syndrome: correlation between clinical features and molecular diagnosis [Internet]. European journal of neurology. 2022 ; 29( 3): 833-842.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1111/ene.15173