Mitochondrial neuropathy in pediatric patients carrying mtDNA, POLG1, SURF1, and PDHA1 mutations. Journal of Medical Biomedical and Applied Sciences, [S. l.], v. 6, n. 9, p. 146, 2018. DOI: 10.15520/jmbas.v6i9.150. Disponível em: https://jmbm.in/index.php/jmbas/article/view/150. Acesso em: 23 10月. 2026.