threonine has been researched along with alpha-LCAT Deficiency in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Goñi Ros, N; González-Tarancón, R; Puzo Bayod, M; Puzo Foncillas, J; Salvador-Ruperez, E; Sienes Bailo, P | 1 |
| Hill, JS; O, K; Pritchard, PH; Wang, X | 1 |
2 other study(ies) available for threonine and alpha-LCAT Deficiency
| Article | Year |
|---|---|
A novel pathogenic variant in LCAT causing FLD. A case report.
Topics: Cholesterol, HDL; Corneal Opacity; Histidine; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Lecithins; Male; Phosphatidylcholine-Sterol O-Acyltransferase; Sterol O-Acyltransferase; Threonine | 2022 |
Lecithin:cholesterol acyltransferase deficiency: identification of a causative gene mutation and a co-inherited protein polymorphism.
Topics: Alanine; Amino Acid Sequence; Arginine; Base Sequence; Cystine; Humans; Lecithin Cholesterol Acyltransferase Deficiency; Lipoproteins; Molecular Sequence Data; Mutation; Phosphatidylcholine-Sterol O-Acyltransferase; Polymorphism, Genetic; Threonine | 1993 |