Source:http://linkedlifedata.com/resource/lhgdn/association:23270
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
LRRK2 G2019S mutation occurred in patients with parkinsonism associated with either typical brainstem LB pathology or non-specific nigral degeneration, were not encountered in other neurodegenerative disorders associated with synuclein and tau deposition.
|
| lhgdn:mesh_code |
D020734
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |