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Q33382898-410223B4-8A1D-4E80-9D33-3AEA79630B9F
Q33382898-410223B4-8A1D-4E80-9D33-3AEA79630B9F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33382898-410223B4-8A1D-4E80-9D33-3AEA79630B9F
A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities
P2860
Q33382898-410223B4-8A1D-4E80-9D33-3AEA79630B9F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33382898-410223B4-8A1D-4E80-9D33-3AEA79630B9F
rank
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type
BestRank
Statement
wasDerivedFrom
559f102ae6b8ff19f05861b4df4751d6c78c7c96
P2860
Familial apolipoprotein AI and apolipoprotein CIII deficiency. Subclass distribution, composition, and morphology of lipoproteins in a disorder associated with premature atherosclerosis.