Matches in Nanopublications for { ?s ?p "[Thus, the phenotype associated with the unique combination of mutations uncovered in both patients expands the spectrum of disease associated with TMPRSS6 mutations to include iron deficiency anemia that is accompanied by hyperferritinemia at initial presentation and is responsive to continued oral iron therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Thus, the phenotype associated with the unique combination of mutations uncovered in both patients expands the spectrum of disease associated with TMPRSS6 mutations to include iron deficiency anemia that is accompanied by hyperferritinemia at initial presentation and is responsive to continued oral iron therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_assertion description "[Thus, the phenotype associated with the unique combination of mutations uncovered in both patients expands the spectrum of disease associated with TMPRSS6 mutations to include iron deficiency anemia that is accompanied by hyperferritinemia at initial presentation and is responsive to continued oral iron therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977557.RAs3PzZmPYh35XlS2EaTAWfVVLgrVOc_dmRoTR00NAcDQ130_provenance.
- NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_assertion description "[Thus, the phenotype associated with the unique combination of mutations uncovered in both patients expands the spectrum of disease associated with TMPRSS6 mutations to include iron deficiency anemia that is accompanied by hyperferritinemia at initial presentation and is responsive to continued oral iron therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1043887.RA98UMMKi-Lym4w3WsVJo2BQrr-f9y6Hpo8xxWjx79OrE130_provenance.