1-carboxyglutamic acid has been researched along with Factor X Deficiency in 1 studies
| 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 | Studies |
|---|---|
| Ambo, H; Ikeda, Y; Kikuchi, M; Moriki, T; Murakami, H; Murata, M; Watanabe, R; Yokoyama, K; Zama, T | 1 |
1 other study(ies) available for 1-carboxyglutamic acid and Factor X Deficiency
| Article | Year |
|---|---|
A family with hereditary factor X deficiency with a point mutation Gla32 to Gln in the Gla domain (factor X Tokyo).
Topics: 1-Carboxyglutamic Acid; Adult; Factor X; Factor X Deficiency; Female; Heterozygote; Homozygote; Humans; Male; Pedigree; Point Mutation | 1999 |