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Q33891534-6372DE29-6FF0-4497-82CB-FB959E3FBCF2
Q33891534-6372DE29-6FF0-4497-82CB-FB959E3FBCF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33891534-6372DE29-6FF0-4497-82CB-FB959E3FBCF2
Genetic and phenotypic heterogeneity in familial lecithin: cholesterol acyltransferase (LCAT) deficiency. Six newly identified defective alleles further contribute to the structural heterogeneity in this disease.
P2860
Q33891534-6372DE29-6FF0-4497-82CB-FB959E3FBCF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33891534-6372DE29-6FF0-4497-82CB-FB959E3FBCF2
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type
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wasDerivedFrom
57b9a02aa57ecccc65274a78894bda85e6185d69
P2860
Familial apolipoprotein AI and apolipoprotein CIII deficiency. Subclass distribution, composition, and morphology of lipoproteins in a disorder associated with premature atherosclerosis.