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| 1989 | 1 |
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A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacities.
J Clin Invest. 1991 Jan;87(1):371-6. doi: 10.1172/JCI114997.
J Clin Invest. 1991.
PMID: 1898657
Free PMC article.
Production of human recombinant proapolipoprotein A-I in Escherichia coli: purification and biochemical characterization.
Moguilevsky N, Roobol C, Loriau R, Guillaume JP, Jacobs P, Cravador A, Herzog A, Brouwers L, Scarso A, Gilles P, et al.
Moguilevsky N, et al.
DNA. 1989 Jul-Aug;8(6):429-36. doi: 10.1089/dna.1.1989.8.429.
DNA. 1989.
PMID: 2673706
Free article.
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