Early genetic diagnosis of thymidine kinase 2-related mitochondrial DNA depletion syndrome in a neonate with respiratory failure: A rare case highlighting the role of early genetic diagnosis and ethical decision-making. Indian Journal of Case Reports, [S. l.], v. 12, n. 4, 2026. DOI: 10.32677/ijcr.v12i4.8152. Disponível em: https://mansapublishers.com/ijcr/article/view/8152. Acesso em: 18 apr. 2026.