PedAM
Pediatric Disease Annotations & Medicines
| Disease | rett syndrome |
| Phenotype | C0036346|childhood schizophrenia |
| Sentences | 1 |
| PubMedID- 23750231 | Similarly, mutations in the x-linked mecp2 gene, which encodes the transcriptional regulator methyl-cpg-binding protein 2 (mecp2), result in one of the asds, the rett syndrome, and are associated with childhood schizophrenia [22]–[26]. |
Page: 1