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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343433/
https://www.ncbi.nlm.nih.gov/pubmed/22476991
http://dx.doi.org/10.3349/ymj.2012.53.3.495

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343433/
https://www.ncbi.nlm.nih.gov/pubmed/22476991
http://dx.doi.org/10.3349/ymj.2012.53.3.495

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