Source:http://linkedlifedata.com/resource/lhgdn/association:53906
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Results suggest that the Cockayne syndrome phenotype results from C-terminal truncations in the XPG (xeroderma pigmentosum) gene in mice and humans.
|
| lhgdn:mesh_code |
D003057
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |