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

Owen, J.S.; Wiebusch, H.; Cullen, P.; Watts, G.F.; Lima, V.L.; Funke, H.; Assmann, G.

Human Mutation 8(1): 79-82

1996


ISSN/ISBN: 1059-7794
PMID: 8807342
DOI: 10.1002/(sici)1098-1004(1996)8:1<79::aid-humu13>3.0.co;2-o
Accession: 045603723

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