Matches in Nanopublications for { ?s ?p "[We have shown that Tangier disease, a rare and severe form of HDL deficiency characterised by a biochemical defect in cellular cholesterol efflux, is caused by mutations in the ATP-binding-cassette (ABC1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_assertion description "[We have shown that Tangier disease, a rare and severe form of HDL deficiency characterised by a biochemical defect in cellular cholesterol efflux, is caused by mutations in the ATP-binding-cassette (ABC1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213749.RAUoCldK4EqpJZ0c5jTXnFhy7bNTXDRJPozrApxhZwN_o130_provenance.
- assertion description "[We have shown that Tangier disease, a rare and severe form of HDL deficiency characterised by a biochemical defect in cellular cholesterol efflux, is caused by mutations in the ATP-binding-cassette (ABC1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP586419.RAQsxdkl9-W2Cbwm4Qqf3Ka9aKzfdDWfpkSfe3Ml-ijXQ130_assertion description "[We have shown that Tangier disease, a rare and severe form of HDL deficiency characterised by a biochemical defect in cellular cholesterol efflux, is caused by mutations in the ATP-binding-cassette (ABC1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586419.RAQsxdkl9-W2Cbwm4Qqf3Ka9aKzfdDWfpkSfe3Ml-ijXQ130_provenance.
- assertion description "[We have shown that Tangier disease, a rare and severe form of HDL deficiency characterised by a biochemical defect in cellular cholesterol efflux, is caused by mutations in the ATP-binding-cassette (ABC1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.