Source:http://linkedlifedata.com/resource/lhgdn/association:46941
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
analysis of missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val) [letter]
|
| lhgdn:mesh_code |
D002836
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |