Ranjan, Ankit, M. Shahbaz Alam, Vinod Kumar, Snigdha Samanta, Rajesh Kumar, and Khalid M. Saifullah. 2023. “Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 Secondary to Phosphatidylinositol Glycan Class T Mutation: A Neonatal Case Report”. International Journal of Contemporary Pediatrics 10 (3):394-97. https://doi.org/10.18203/2349-3291.ijcp20230443.