1. Agorastos, J., Fox, C., Harry, D. S. and McIntyre, N. Lecithin-cholesterol acyltransferase and the lipoprotein abnormalities of obstructive jaundice.Clin. Sci. Mol. Med. 54 (1978) 369–379
2. Angelin, B. and Carlson, L. A. Bile acids and plasma high-density lipoproteins: bilary lipid metabolism in fish-eye disease.Eur. J. Clin. Invest. 16 (1986) 157–162
3. Azoulay, M., Henry, I., Tata, F., Weil, D., Grezchik, K. H., Chaves, M. E., McIntyre, N., Williamson, R., Humphries, S. E. and Junien, C. The structural gene for lecithin: cholesterol acyltransferase (LCAT) maps to 16q22′.Ann. Hum. Genet. 51 (1987) 129–136
4. Bethell, W., McCulloch, C. and Ghosh, M. Lecithin-cholesterol acyltransferase deficiency: light and electron microscopic findings from two corneas.Can. J. Ophthalmol. 10 (1975) 494–501
5. Bron, A. J., Lloyd, J. K., Fosbrooke, A. S., Winder, A. F. and Tripathi, R. C. Primary LCAT deficiency disease.Lancet 1 (1975) 928–929