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Fig. 1 | Lipids in Health and Disease

Fig. 1

From: Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia

Fig. 1

LCAT mutations found in a Chilean patient with hypoalphalipoproteinemia and her relatives. (a) Each family member is shown with his/her genotype in for p.V333 M and p.M404 V mutations. Proband is indicated by a black arrow. (b) The chart shows FPLC fractions for HDL, LDL and VLDL lipoproteins in the proband, indicating near-absence of HDL-lipoproteins and very low levels of LDL-lipoproteins

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