Etarhuni, S. . ., & Sharfddin, A. . . (2025). First Report of PIGT Mutant Among the Libyan Population that Cause Multiple Congenital Anomalies, Hypotonia, Seizure Syndrome (MCAHS3) by A New Gene Mutation: A CASE REPORT. مجلة تريبوليتانا الطبية, 10(2), 31–28. استرجع في من https://uot.edu.ly/journals/index.php/tmj/article/view/1787