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    Hum Mutat. 1996;8(1):79-82.

    Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT gene.

    Owen JS, Wiebusch H, Cullen P, Watts GF, Lima VL, Funke H, Assmann G.

    Source

    University Department of Medicine, Royal Free Hospital School of Medicine, London, UK.

    PMID:
    8807342
    [PubMed - indexed for MEDLINE]

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