Mendonca, Rodrigo de Holanda; Matsui Junior, Ciro; Polido, Graziela Jorge; Silva, Andre Macedo Serafim; Kulikowski, Leslie; Dias, Alexandre Torchio; Zanardo, Evelin Aline; Marques Júnior, Wilson 
; Tomaselli, Pedro José; Kok, Fernando ; Reed, Umbertina Conti ; Zanoteli, Edmar
Fonte: Neurology-genetics. Unidades: FMRP, FM
Assuntos: ATROFIA MUSCULAR, FENÓTIPOS, GENES
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ABNT
MENDONCA, Rodrigo de Holanda et al. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy. Neurology-genetics, v. 6, n. 5, 2020Tradução . . Disponível em: https://doi.org/10.1212/NXG.0000000000000505. Acesso em: 24 out. 2025.APA
Mendonca, R. de H., Matsui Junior, C., Polido, G. J., Silva, A. M. S., Kulikowski, L., Dias, A. T., et al. (2020). Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy. Neurology-genetics, 6( 5). doi:10.1212/NXG.0000000000000505NLM
Mendonca R de H, Matsui Junior C, Polido GJ, Silva AMS, Kulikowski L, Dias AT, Zanardo EA, Marques Júnior W, Tomaselli PJ, Kok F, Reed UC, Zanoteli E. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy [Internet]. Neurology-genetics. 2020 ; 6( 5):[citado 2025 out. 24 ] Available from: https://doi.org/10.1212/NXG.0000000000000505Vancouver
Mendonca R de H, Matsui Junior C, Polido GJ, Silva AMS, Kulikowski L, Dias AT, Zanardo EA, Marques Júnior W, Tomaselli PJ, Kok F, Reed UC, Zanoteli E. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy [Internet]. Neurology-genetics. 2020 ; 6( 5):[citado 2025 out. 24 ] Available from: https://doi.org/10.1212/NXG.0000000000000505
