hawkinsin has been researched along with 4 Hydroxyphenylpyruvate Dioxygenase Deficiency Disease 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 |
|---|---|
| Bodamer, OA; Item, CB; Jalan, A; Lichtarge, O; Mihalek, I; Muhl, A; Vodopiutz, J | 1 |
| Awata, H; Boneh, A; Danks, DM; Endo, F; Matsuda, I; Matsuura, T; Milovac, T; Ploechl, E; Scott, CR; Tomoeda, K | 1 |
2 other study(ies) available for hawkinsin and 4 Hydroxyphenylpyruvate Dioxygenase Deficiency Disease
| Article | Year |
|---|---|
Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia III.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Amino Acids, Sulfur; Cyclohexenes; DNA; Genetic Carrier Screening; Humans; Infant; Models, Molecular; Polymerase Chain Reaction; Protein Conformation; Tyrosinemias | 2007 |
Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria.
Topics: 4-Hydroxyphenylpyruvate Dioxygenase; Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Base Sequence; Cyclohexenes; DNA; DNA Mutational Analysis; Family Health; Female; Humans; Infant; Male; Mutation; Mutation, Missense; Pedigree; Tyrosinemias | 2000 |