Matches in Nanopublications for { ?s ?p "[Familial lecithin cholesterol acyltransferase (LCAT) deficiency is a rare inherited enzyme deficiency characterized by widespread disturbance of lipid metabolism and infiltration of many organs, including kidneys by lipids; usually it results in death from renal failure in the fourth or fifth decades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP272587.RAQhqarwzBUnje33CginEXLY881VQbiyiKZcxQPFIUfnU130_assertion description "[Familial lecithin cholesterol acyltransferase (LCAT) deficiency is a rare inherited enzyme deficiency characterized by widespread disturbance of lipid metabolism and infiltration of many organs, including kidneys by lipids; usually it results in death from renal failure in the fourth or fifth decades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272587.RAQhqarwzBUnje33CginEXLY881VQbiyiKZcxQPFIUfnU130_provenance.
- NP355948.RAKrkBX_vXHD8SkzlqpqDUtolsiPucb5H1elgcL0h_Qko130_assertion description "[Familial lecithin cholesterol acyltransferase (LCAT) deficiency is a rare inherited enzyme deficiency characterized by widespread disturbance of lipid metabolism and infiltration of many organs, including kidneys by lipids; usually it results in death from renal failure in the fourth or fifth decades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355948.RAKrkBX_vXHD8SkzlqpqDUtolsiPucb5H1elgcL0h_Qko130_provenance.
- assertion description "[Familial lecithin cholesterol acyltransferase (LCAT) deficiency is a rare inherited enzyme deficiency characterized by widespread disturbance of lipid metabolism and infiltration of many organs, including kidneys by lipids; usually it results in death from renal failure in the fourth or fifth decades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_assertion description "[Familial lecithin cholesterol acyltransferase (LCAT) deficiency is a rare inherited enzyme deficiency characterized by widespread disturbance of lipid metabolism and infiltration of many organs, including kidneys by lipids; usually it results in death from renal failure in the fourth or fifth decades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532322.RAw9LdIggXvpfd9T6yUXiweC3QxQWyBnRdw4tzbazozRY130_provenance.
- NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_assertion description "[Familial lecithin cholesterol acyltransferase (LCAT) deficiency is a rare inherited enzyme deficiency characterized by widespread disturbance of lipid metabolism and infiltration of many organs, including kidneys by lipids; usually it results in death from renal failure in the fourth or fifth decades.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1307733.RA9tGuGcFJ9-cJrl-LD_49vVe_adfSjU427nK5OYXGBtY130_provenance.