Source:http://linkedlifedata.com/resource/lhgdn/association:22076
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
In human heterozygotes of CRB1 mutations (parents of offspring with Leber congenital amaurosis), distinctive regional retinal dysfunctions were found by multifocal ERG (electroretinography) measurements
|
| lhgdn:mesh_code |
D001766
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |