IDENTIFICATION OF THE HOMOZYGOUS MISSENSE MUTATION IN THE LECITHIN-CHOLESTEROL-ACYLTRANSFERASE (LCAT) GENE, CAUSING LCAT FAMILIAL DEFICIENCY IN 2 FRENCH PATIENTS

Authors
DORVAL I JEZEQUEL P DUBOURG C CHAUVEL B LEPOGAMP P LEGALL JY
Citation
I. Dorval et al., IDENTIFICATION OF THE HOMOZYGOUS MISSENSE MUTATION IN THE LECITHIN-CHOLESTEROL-ACYLTRANSFERASE (LCAT) GENE, CAUSING LCAT FAMILIAL DEFICIENCY IN 2 FRENCH PATIENTS, Atherosclerosis, 105(2), 1994, pp. 251-252
Citations number
4
Categorie Soggetti
Cardiac & Cardiovascular System
Journal title
Atherosclerosis → ACNP
ISSN journal
00219150
Volume
105
Issue
2
Year of publication
1994
Pages
251 - 252
Database
ISI
SICI code
0021-9150(1994)105:2<251:IOTHMM>2.0.ZU;2-C