Source:http://linkedlifedata.com/resource/lhgdn/association:47476
Predicate | Object |
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lhgdn:found_in | |
lhgdn:geneRifSource |
study reports a new molecular defect in a family with true prothrombin deficiency; the mother was homozygous for a mutation Arg-Gln in position -39 of the propeptide controlled by exon 1; the son was heterozygosity for the same mutation
|
lhgdn:mesh_code |
D007020
|
lhgdn:associationIdType | |
lhgdn:umls_code |