PRADHAN, R.; GUPTA, J. Wilson’s disease: A rare autosomal recessive disorder of copper metabolism. Journal of Chitwan Medical College, [S. l.], v. 4, n. 2, p. 51–53, 2014. Disponível em: https://www.nepjol.info/index.php/JCMC/article/view/10866. Acesso em: 19 apr. 2024.