GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease - 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 (Neuromuscular Disorders, 2021)