phenylalanine has been researched along with Factor VII Deficiency in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chafa, O; Fischer, AM; Reghis, A; Tapon-Bretaudiere, J | 1 |
| Fromovich-Amit, Y; Landau, M; Rosa, JP; Rosenberg, N; Seligsohn, U; Zivelin, A | 1 |
2 other study(ies) available for phenylalanine and Factor VII Deficiency
| Article | Year |
|---|---|
Homozygous nonsense mutation (Cys72-->stop) in the human F7 gene: a not life-threatening mutation despite the absence of circulating factor VII.
Topics: Adult; Coagulants; Codon, Nonsense; Codon, Terminator; Cysteine; Factor VII; Factor VII Deficiency; Family Health; Female; Genotype; Heterozygote; Homozygote; Humans; Infant; Male; Mutation; Phenotype; Phenylalanine; Risk | 2005 |
Of four mutations in the factor VII gene in Tunisian patients, one novel mutation (Ser339Phe) in three unrelated families abrogates factor X activation.
Topics: DNA Mutational Analysis; Factor VII; Factor VII Deficiency; Factor X; Female; Humans; Male; Models, Molecular; Mutation; Pedigree; Phenylalanine; Serine; Tunisia | 2005 |