Figueiredo, Fernanda Barbosa 
; Silva Junior, Wilson Araújo da ; Giuliatti, Silvana ; Tomaselli, Pedro José; Lourenço, Charles Marques; Gouvêa, Silmara Paula; Covaleski, Anna Paula Paranhos Miranda; Hallak, Jaime Eduardo Cecilio ; Marques Júnior, Wilson
Source: Neuromuscular Disorders. Unidade: FMRP
Subjects: DOENÇAS DO SISTEMA NERVOSO, DOENÇAS DEGENERATIVAS, MUTAÇÃO GENÉTICA
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FIGUEIREDO, Fernanda Barbosa et al. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, v. 31, n. 6, p. 505-511, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2021.03.005. Acesso em: 13 jun. 2024.APA
Figueiredo, F. B., Silva Junior, W. A. da, Giuliatti, S., Tomaselli, P. J., Lourenço, C. M., Gouvêa, S. P., et al. (2021). GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease. Neuromuscular Disorders, 31( 6), 505-511. doi:10.1016/j.nmd.2021.03.005NLM
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005Vancouver
Figueiredo FB, Silva Junior WA da, Giuliatti S, Tomaselli PJ, Lourenço CM, Gouvêa SP, Covaleski APPM, Hallak JEC, Marques Júnior W. GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease [Internet]. Neuromuscular Disorders. 2021 ; 31( 6): 505-511.[citado 2024 jun. 13 ] Available from: https://doi.org/10.1016/j.nmd.2021.03.005
