RANJAN, A.; ALAM, M. S.; KUMAR, V.; SAMANTA, S.; KUMAR, R.; SAIFULLAH , K. M. Multiple congenital anomalies-hypotonia-seizures syndrome 3 secondary to phosphatidylinositol glycan class T mutation: a neonatal case report. International Journal of Contemporary Pediatrics, [S. l.], v. 10, n. 3, p. 394–397, 2023. DOI: 10.18203/2349-3291.ijcp20230443. Disponível em: https://www.ijpediatrics.com/index.php/ijcp/article/view/5132. Acesso em: 29 apr. 2026.