FERREIRA GONÇALVES, C.; LIPARI PINTO, P.; CLARO, A. R.; COELHO, J.; QUINTAS, S.; RODRIGUES, M.; COSTA, P.; MARGALHA MIRANDA, A.; REBELO, M.; NOGUEIRA, C.; JANEIRO, P.; GASPAR, A. New variant in the FBXL4 gene – leading to mitochondrial DNA depletion syndrome. Journal of Pediatric and Neonatal Individualized Medicine (JPNIM), Quartu Sant’Elena (CA, Italy), v. 13, n. 1, p. e130111, 2024. DOI: 10.7363/130111. Disponível em: https://jpnim.com/index.php/jpnim/article/view/e130111. Acesso em: 16 jul. 2024.