Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome
OBJECTIVE: Rett syndrome (RTT) is a neurodevelopmental disorder that represents one of the most common genetic causes of mental retardation in girls. The aim of this study was to investigate the correlation between MECP2 genotype and phenotype and thereby not only to provide assistance for clinical...
| Publié dans: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 47(2009), 2 vom: 03. Feb., Seite 124-8 |
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| Auteur principal: | |
| Autres auteurs: | , , , , , |
| Format: | Article |
| Langue: | Chinese |
| Publié: |
2009
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| Accès à la collection: | Zhonghua er ke za zhi = Chinese journal of pediatrics |
| Sujets: | English Abstract Journal Article MECP2 protein, human Methyl-CpG-Binding Protein 2 |