Source:http://linkedlifedata.com/resource/lhgdn/association:53558
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Data suggest that the microcephaly observed in patients with MCPH1 deficiencies is due to disruption of the ATR-BRCA1-Chk1 signaling pathway that is also disrupted in Seckel syndrome patients.
|
| lhgdn:mesh_code |
D008831
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |