Source:http://linkedlifedata.com/resource/lhgdn/association:29782
Predicate | Object |
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lhgdn:found_in | |
lhgdn:geneRifSource |
Sequencing of the hydroxymethylbilane synthase and uroporphyrinogen decarboxylase genes confirmed the relatively rare diagnosis of dual porphyria, and revealed a novel uroporphyrinogen decarboxylase mutation
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lhgdn:mesh_code |
D011164
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lhgdn:associationIdType | |
lhgdn:umls_code |