Source:http://linkedlifedata.com/resource/lhgdn/association:32404
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Data show that a single nucleotide variant in the Fragile X Mental Retardation Protein-1 CGG repeat results in a " Pseudodeletion " and is not associated with the fragile X syndrome phenotype.
|
| lhgdn:mesh_code |
D005600
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |