GDAP1 mutations are frequent among Brazilian patients with autosomal recessive axonal Charcot-Marie-Tooth disease
| Autor: | Figueiredo, Fernanda Barbosa, Silva, Wilson Araújo, Jr., Giuliatti, Silvana, Tomaselli, Pedro José, Lourenço, Charles Marques, Gouvêa, Silmara de Paula, Covaleski, Anna Paula Paranhos Miranda, Hallak, Jaime E., Marques, Wilson, Jr. |
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| Zdroj: | In Neuromuscular Disorders June 2021 31(6):505-511 |
| Databáze: | ScienceDirect |
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