[1]
Jali, N. et al. 2025. Genetically Confirmed Schwartz–Jampel Syndrome: An Ultra-Rare Case of Congenital Myotonia with Osteochondrodysplasia from India. International Journal of Medical Students. 13, (Dec. 2025), S270. DOI:https://doi.org/10.5195/ijms.2025.4063.