Source:http://linkedlifedata.com/resource/lhgdn/association:63066
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
patients with GRN mutations: have a shorter disease duration (with the exception of FTD-MND); present bvFTLD, language output impairment or with CBS; have parietal lobe dysfunction; and have evidence of asymmetrical brain atrophy on MR imaging.
|
| lhgdn:mesh_code |
D001284
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |