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Q28263895-5DDB384E-2242-4F8D-84D2-FEBE93503F2D
Q28263895-5DDB384E-2242-4F8D-84D2-FEBE93503F2D
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Statement
http://www.wikidata.org/entity/statement/Q28263895-5DDB384E-2242-4F8D-84D2-FEBE93503F2D
The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families
P2860
Q28263895-5DDB384E-2242-4F8D-84D2-FEBE93503F2D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28263895-5DDB384E-2242-4F8D-84D2-FEBE93503F2D
rank
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Statement
wasDerivedFrom
24861d10ff21f89c0761902358657dbace82aa57
P2860
A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities