1. Impaired secretion by the liver and intestine of lipoproteins containing apolipoprotein B probably underlies the intestinal malabsorption and the plasma lipoprotein abnormalities seen in abetaand hypobeta-lipoproteinaemia. The mechanism for the other clinical features is unknown. They are unlikely to be a consequence of LCAT deficiency as they are not observed in familial LCAT deficiency,1974
2. Acanthocytosis and neurological disease;Aminoff, M.J.;Brain,1972
3. Malformation of the erythrocytes in a case of atypical retinitis pigmentosa;Bassen, F.A.; Kornzweig, A.L.;Blood,1950
4. Classification of hyperlipidaemias and hyperlipoproteinaemias;Beaumont, J.L.; Carlson, L.A.; Cooper, G.R.; Fejfar, Z.; Fredrickson, D.S.; Strasser, T.;Bulletin of the World Health Organisation,1970
5. The genetic relationship of abetalipoproteinemia and hypobetalipoproteinemia: a report of the occurrence of both diseases within the same family;Biemer, J.I.; McCammon, R.E.;Journal ofLaboratory and Clinical Medicine,1975