Source:http://linkedlifedata.com/resource/lhgdn/association:17037
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Mutant 5-residue polyalanine expansion of FoxL2 leads to recessive inheritance of blepharophimosis syndrome associated with ovarian dysfunction.
|
| lhgdn:mesh_code |
D016569
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |