CHD2-related epilepsy: novel mutations and new phenotypes

Jiaoyang Chen1, Jing Zhang1, Aijie Liu1

  • 1Department of Pediatrics, Peking University First Hospital, Beijing, China.

Summary

This study refines understanding of chromodomain helicase DNA-binding protein 2 (CHD2) mutations in epilepsy, identifying new mutations and phenotypes like West syndrome. Findings highlight the diverse clinical spectrum of CHD2-related epilepsy.

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