Correlation between clinical features and MECP2 gene mutations in patients with Rett syndrome
Background: Rett syndrome is a progressive neurodevelopment disorder which mainly affects females and is a common cause of mental retardation. Loss of purposeful hand movements, regression of acquired cognitive and motor skills and autistic features are the main criteria associated with this disorde...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
SpringerOpen
2015-03-01
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| Series: | Egyptian Pediatric Association Gazette |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S1110663815000026 |