<it>De novo </it>deletion in <it>MECP2 </it>in a monozygotic twin pair: a case report
<p>Abstract</p> <p>Background</p> <p>Rett syndrome (RTT) is a severe, progressive, neurodevelopmental disorder predominantly observed in females that leads to intellectual disability. Mutations and gross rearrangements in <it>MECP2 </it>account for a large p...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2011-08-01
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| Series: | BMC Medical Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2350/12/113 |