proline and Lecithin Cholesterol Acyltransferase Deficiency

proline has been researched along with Lecithin Cholesterol Acyltransferase Deficiency in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Chauvel, B; Dorval, I; Dubourg, C; Jezequel, P; Le Gall, JY; Le Pogamp, P	1

Other Studies

1 other study(ies) available for proline and Lecithin Cholesterol Acyltransferase Deficiency

Article	Year
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patients. Atherosclerosis, 1994, Volume: 105, Issue:2 Topics: Adult; Base Sequence; Exons; Female; Homozygote; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Leucine; Male; Molecular Sequence Data; Phosphatidylcholine-Sterol O-Acyltransferase; Point Mutation; Polymerase Chain Reaction; Proline	1994

Article

Year

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

Atherosclerosis, 1994, Volume: 105, Issue:2

Topics: Adult; Base Sequence; Exons; Female; Homozygote; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Leucine; Male; Molecular Sequence Data; Phosphatidylcholine-Sterol O-Acyltransferase; Point Mutation; Polymerase Chain Reaction; Proline

1994