Source:http://linkedlifedata.com/resource/lhgdn/association:22969
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Defective cellular localization of mutant ATP7B in Wilson?s disease and hepatoma cell lines/was trapped in endoplasmic reticulum/ATP7B mutants showed a diffuse, clustered, cytoplasmic pattern.
|
| lhgdn:mesh_code |
D006528
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |