MUHAMMAD AKRAM CHOOHAN; ISHTIAQ AHMED; SHAHZADA KHURRAM SYED; MUHAMMAD NAEEM. SCN1A gene mutation: A rising cause of human epilepsy syndrome. Journal of Contemporary Pharmacy, [S. l.], v. 6, n. 1, p. 32–40, 2022. DOI: 10.56770/jcp2022615. Disponível em: https://ammanif.com/journal/jcp/index.php/home/article/view/38. Acesso em: 27 nov. 2024.