YOGANATHAN, S.; SUDHAKAR, S. V.; THOMAS, M. M.; DUTTA, A. K.; DANDA, S.; CHANDRAN, M. Novel imaging finding and novel mutation in an infant with molybdenum cofactor deficiency: a mimicker of hypoxic ischaemic encephalopathy. Iranian Journal of Child Neurology, [S. l.], v. 12, n. 2, p. 107–112, 2018. DOI: 10.22037/ijcn.v12i2.12671. Disponível em: https://journals.sbmu.ac.ir/ijcn/article/view/12671. Acesso em: 23 apr. 2024.