Source:http://linkedlifedata.com/resource/lhgdn/association:17883
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
assessed whether 232A-- > G or other BCS1L mutations were present in infants (n = 21) of Finnish origin with severe, lethal disease compatible with mitochondrial disorder
|
| lhgdn:mesh_code |
D028361
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |