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1 Genetic and Epileptic Features in Rett Syndrome

Kim HJ, Kim SH, Kim HD, Lee JS, Lee YM, Koo KY, Lee JS, Kang HC

KMID: 1776982
Yonsei Med J.
2012 May;53(3):495-500.
doi: 10.3349/ymj.2012.53.3.495

PURPOSE: Rett syndrome is a severe neurodevelopmental disorder in females. Most have mutations in the methyl-CpG-binding protein 2 (MECP2) gene (80-90%). Epilepsy is a significant commonly accompanied feature in Rett...

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