A G+1 to C mutation in a donor splice site of intron 2 in the apolipoprotein (apo) C-II gene in a patient with apo C-II deficiency. A possible interaction between apo C-II deficiency and apo E4 in a severly hypertrigyceridemic patient - Okubo, M; Hasegawa, Y; Aoyama, Y; Murase, T (Arthero-sclerosis, 1997)