Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patients

Dorval, I.; Jezequel, P.; Dubourg, C.; Chauvel, B.; Le Pogamp, P.; Le Gall, J.Y.

Atherosclerosis 105(2): 251-252

1994


ISSN/ISBN: 0021-9150
PMID: 8003101
DOI: 10.1016/0021-9150(94)90056-6
Accession: 046317885

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