Source: Neurology-genetics. Unidades: FMRP, FM
Subjects: ATROFIA MUSCULAR, FENÓTIPOS, GENES
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: 03 maio 2024.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 2024 maio 03 ] 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 2024 maio 03 ] Available from: https://doi.org/10.1212/NXG.0000000000000505