Source:http://linkedlifedata.com/resource/lhgdn/association:18310
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
it is reported for the first time that mutations in CABP4 lead to autosomal recessive congenital stationary night blindness
|
| lhgdn:mesh_code |
D009755
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |