PedAM
Pediatric Disease Annotations & Medicines
| Disease | n syndrome |
| Phenotype | C0039730|thalassaemia |
| Sentences | 1 |
| PubMedID- 21505078 | Atrx is a member of the snf2 family of chromatin-remodelling proteins and is mutated in an x-linked mental retardation syndrome associated with alpha-thalassaemia (atr-x syndrome). |
Page: 1