threonine has been researched along with Afibrinogenemia, Congenital in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, Y; Cheng, Y; Duan, X; Liao, Z; Liu, C; Luo, M; Tan, Y; Tang, H; Wang, D; Xie, Y; Xu, S | 1 |
1 other study(ies) available for threonine and Afibrinogenemia, Congenital
| Article | Year |
|---|---|
Fibrinogen Hangzhou: congenital dysfibrinogenemia caused by the novel missense mutation in FGG (γ308Asn→Thr).
Topics: Afibrinogenemia; Asparagine; China; Fibrinogen; Humans; Male; Middle Aged; Mutation, Missense; Threonine | 2014 |