Source:http://linkedlifedata.com/resource/lhgdn/association:23300
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Parkinson disease related to LRRK2 is characterized by typical clinical features, and the similarities between patients with homozygous and heterozygous mutations do not support a gene dosage effect.
|
| lhgdn:mesh_code |
D010300
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |