Matches in Nanopublications for { ?s ?p "[Mutations in the ATP-binding cassette transporter 1 (ABCA1) gene have been recently identified as the molecular defect in Tangier disease (TD) and familial high density lipoprotein deficiency (FHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_assertion description "[Mutations in the ATP-binding cassette transporter 1 (ABCA1) gene have been recently identified as the molecular defect in Tangier disease (TD) and familial high density lipoprotein deficiency (FHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP181095.RA8aAa_pR3hVi8TCtjjSO1tT9gWnnglvFqqMvNuYhuIMA130_provenance.
- NP7213.RA5df9gXbuvUun1TJEpmSNne_6WW_PlR3DHb2rPATFG9g130_assertion description "[Mutations in the ATP-binding cassette transporter 1 (ABCA1) gene have been recently identified as the molecular defect in Tangier disease (TD) and familial high density lipoprotein deficiency (FHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7213.RA5df9gXbuvUun1TJEpmSNne_6WW_PlR3DHb2rPATFG9g130_provenance.
- NP7205.RALQ_eOrArOBaiouSdM60QbwYoesCPUpxzAB1Sa247vL0130_assertion description "[Mutations in the ATP-binding cassette transporter 1 (ABCA1) gene have been recently identified as the molecular defect in Tangier disease (TD) and familial high density lipoprotein deficiency (FHA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7205.RALQ_eOrArOBaiouSdM60QbwYoesCPUpxzAB1Sa247vL0130_provenance.