Determinants of sleep disturbances in Rett syndrome: Novel findings in relation to genotype
Rett syndrome is a rare but severe neurological disorder associated with a mutation in the methyl CpG binding protein 2 (MECP2) gene. Sleep problems and epilepsy are two of many comorbidities associated with this disorder. This study investigated the prevalence and determinants of sleep problems in...
| Main Authors: | , , , , , , |
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| Format: | Journal Article |
| Published: |
John Wiley & Sons, Inc.
2016
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| Online Access: | http://hdl.handle.net/20.500.11937/29045 |