Source:http://linkedlifedata.com/resource/lhgdn/association:39161
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Homozygosity at codon 129 suggests that codon 129 coupled with the mutation as well as that located on the normal allele can modify major phenotypic features of Creutzfeldt Jakob disease.
|
| lhgdn:mesh_code |
D007562
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |