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. Tripolitana Medical Journal [انترنت]. 4 أبريل، 2025 [وثق 19 أبريل، 2026];10(2):31-28. موجود في: https://journals.uot.edu.ly/index.php/tmj/article/view/1787