Source:http://linkedlifedata.com/resource/lhgdn/association:32414
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Fragile X syndrome offers a unique molecular model for autism since FMRP regulates the translation of many other genes involved in synaptic formation and plasticity which should be natural targets for further exploration.
|
| lhgdn:mesh_code |
D005600
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |