Cites del registre
Cita APA (7th ed.)
Funke, H., von Eckardstein, A., Pritchard, P. H., Karas, M., Albers, J. J., & Assmann, G. (1991). 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.
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Cita Chicago (17th ed.)
Funke, H., A. von Eckardstein, P H. Pritchard, M. Karas, J J. Albers, i G. Assmann. "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.
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Cita MLA (9th ed.)
Funke, H., et al. "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.
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Atenció: Aquestes cites poden no estar 100% correctes.