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Etarhuni, S. و 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 (2025), 31–28.