# Neurodevelopmental Disorder and Cortical Myoclonus in ZMYM2 Deficiency

**Authors:** Luca Pollini, Maria Novelli, Lorena Travaglini, Fabiola Panvino, Vincenzo Leuzzi, Francesco Pisani, Serena Galosi

PMC · DOI: 10.1002/mds.70056 · Movement Disorders · 2025-09-24

## Full-text entities

- **Genes:** ZMYM2 (zinc finger MYM-type containing 2) [NCBI Gene 7750] {aka FIM, MYM, NECRC, RAMP, SCLL, ZNF198}
- **Diseases:** Cortical Myoclonus (OMIM:614937), Neurodevelopmental Disorder (MESH:D002658)

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Source: https://tomesphere.com/paper/PMC13001705