OP-066 A mutation leading to rare neurodevelopmental disorder unique to Turkish population

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1. 1Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study2024 · 8 citations
2. 2Genetic and clinical insights into pontocerebellar hypoplasia: Identification of novel variants in an Iranian cohort2026
3. 3Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review2024 · 6 citations
4. 4Pontocerebellar hypoplasia type 7 with multiple congenital anomalies and progressive neurological course: a case report2026
5. 5<scp><i>MINPP1</i></scp>‐Related Pontocerebellar Hypoplasia in Five New Patients: Identification of Three Novel Variants and Further Phenotype Delineation2025