Neuromyopathy due to mitochondrial trifunctional protein deficiency caused by novel HADHA mutation. Indian Journal of Child Health, [S. l.], v. 9, n. 5, p. 84–86, 2022. DOI: 10.32677/ijch.v9i5.3393. Disponível em: https://mansapublishers.com/index.php/ijch/article/view/3393.. Acesso em: 13 apr. 2025.