Congenital myasthenic syndrome: correlation between clinical features and molecular diagnosis (2022)
Estephan, Eduardo P; Zambon, Antonio A; Thompson, Rachel; Polavarapu, Kiran; Jomaa, Danny; Topf, Ana; Helito, Paulo V. P; Moreno, Cristiane Araujo Martins 
; Reed, Umbertina Conti ; Zanoteli, Edmar
Source: European journal of neurology. Unidade: FM
Subjects: DOENÇAS NEUROMUSCULARES, MIASTENIA GRAVIS, IMAGEM POR RESSONÂNCIA MAGNÉTICA, DIAGNÓSTICO POR IMAGEM
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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: 01 out. 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 out. 01 ] 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 out. 01 ] Available from: https://doi.org/10.1111/ene.15173
