ETARHUNI, S. . .; SHARFDDIN, A. . . 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, [S. l.], v. 10, n. 2, p. 31–28, 2025. Disponível em: https://journals.uot.edu.ly/index.php/tmj/article/view/1787. Acesso em: 31 2026.