JALI, Nandita; MAGAR, Suvarna; TRIKHA, Tanya; VAIDYA, Varsha; VAIDYA, Viranchi. Genetically Confirmed Schwartz–Jampel Syndrome: An Ultra-Rare Case of Congenital Myotonia with Osteochondrodysplasia from India. International Journal of Medical Students, [S. l.], v. 13, p. S270, 2025. DOI: 10.5195/ijms.2025.4063. Disponível em: https://ijms.info/IJMS/article/view/4063. Acesso em: 31 dec. 2025.