Source:http://linkedlifedata.com/resource/lhgdn/association:17039
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Novel mutations in the FOXL2 gene from Blepharophimosis syndrome patients have been found which confirm the existence of two previously described mutational hotspots.
|
| lhgdn:mesh_code |
D016569
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |