Source:http://linkedlifedata.com/resource/lhgdn/association:32409
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
A mosaic deletion of 1, 013, 395 bp in FMR1 was found (using high-density X chromosome microarray analysis followed by sequencing of the deletion breakpoints) to be the cause of Fragile X syndrome.
|
| lhgdn:mesh_code |
D005600
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |