Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis
OBJECTIVE: Rett syndrome (RTT) is a neurodevelopmental disorder which causes severe mental retardation. This study aimed at elucidating clinical features of 66 Chinese RTT cases diagnosed by The Department of Pediatric Neurology, Peking University First Hospital since 1987, and at analysis of the Me...
| Veröffentlicht in: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 42(2004), 4 vom: 24. Apr., Seite 252-5 |
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| 1. Verfasser: | |
| Weitere Verfasser: | , , |
| Format: | Aufsatz |
| Sprache: | Chinese |
| Veröffentlicht: |
2004
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| Zugriff auf das übergeordnete Werk: | Zhonghua er ke za zhi = Chinese journal of pediatrics |
| Schlagworte: | English Abstract Journal Article Research Support, Non-U.S. Gov't Chromosomal Proteins, Non-Histone DNA-Binding Proteins MECP2 protein, human Methyl-CpG-Binding Protein 2 Repressor Proteins Carnitine S7UI8SM58A |