Source:http://linkedlifedata.com/resource/lhgdn/association:32376
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Abnormal development of specific brain regions characterizes a neuroanatomic phenotype associated with fragile X syndrome and may mediate the effects of FMR1 gene mutations on the cognitive and behavioral features of the disorder.
|
| lhgdn:mesh_code |
D005600
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |