Genetic and Epileptic Features in Rett Syndrome

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 syndrome. Our study was aimed at comprehensive analysis of genetic and clinical fea...

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Detalhes bibliográficos
Main Authors: Kim, Hyo Jeong, Kim, Shin Hye, Kim, Heung Dong, Lee, Joon Soo, Lee, Young-Mock, Koo, Kyo Yeon, Lee, Jin Sung, Kang, Hoon-Chul
Formato: Artigo
Idioma:Inglês
Publicado em: Yonsei University College of Medicine 2012
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3343433/
https://ncbi.nlm.nih.gov/pubmed/22476991
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3349/ymj.2012.53.3.495
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