Familial high-density-lipoprotein deficiency causing corneal opacities (fish eye disease) in a family of Dutch descent

scientific article published on 01 April 1992

Familial high-density-lipoprotein deficiency causing corneal opacities (fish eye disease) in a family of Dutch descent is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1111/J.1365-2796.1992.TB00953.X
P698PubMed publication ID1588268

P2093author name stringJ. J. Albers
J. J. Frohlich
P. H. Pritchard
D. W. Erkelens
J. A. Kuivenhoven
J. J. Kastelein
P433issue4
P407language of work or nameEnglishQ1860
P921main subjecteye diseaseQ3041498
P304page(s)413-419
P577publication date1992-04-01
P1433published inJournal of Internal MedicineQ6295387
P1476titleFamilial high-density-lipoprotein deficiency causing corneal opacities (fish eye disease) in a family of Dutch descent
P478volume231

Reverse relations

cites work (P2860)
Q34386276A unique genetic and biochemical presentation of fish-eye disease
Q44361735Deletion of N-terminal amino acids from human lecithin:cholesterol acyltransferase differentially affects enzyme activity toward alpha- and beta-substrate lipoproteins
Q73359069Fish-eye disease: structural and in vivo metabolic abnormalities of high-density lipoproteins
Q34021570Lecithin: cholesterol acyltransferase--from biochemistry to role in cardiovascular disease
Q43719479Lecithin:cholesterol acyl transferase G30S: association with atherosclerosis, hypoalphalipoproteinemia and reduced in vivo enzyme activity
Q36145188Lecithin:cholesterol acyltransferase: old friend or foe in atherosclerosis?
Q47788413Lipid-free apolipoprotein (apo) A-I is converted into alpha-migrating high density lipoproteins by lipoprotein-depleted plasma of normolipidemic donors and apo A-I-deficient patients but not of Tangier disease patients

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