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: | Boban, S., Wong, K., Epstein, A., Anderson, B., Murphy, N., Downs, Jennepher, Leonard, H. |
|---|---|
| Format: | Journal Article |
| Published: |
John Wiley & Sons, Inc.
2016
|
| Online Access: | http://hdl.handle.net/20.500.11937/29045 |
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