thymine has been researched along with Protoporphyria, Erythropoietic in 1 studies
Protoporphyria, Erythropoietic: An autosomal dominant porphyria that is due to a deficiency of FERROCHELATASE (heme synthetase) in both the LIVER and the BONE MARROW, the last enzyme in the 8-enzyme biosynthetic pathway of HEME. Clinical features include mainly neurological symptoms, rarely cutaneous lesions, and elevated levels of protoporphyrin and COPROPORPHYRINS in the feces.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Nakano, H | 1 |
| Nakano, A | 1 |
| Toyomaki, Y | 1 |
| Ohashi, S | 1 |
| Harada, K | 1 |
| Moritsugu, R | 1 |
| Takeda, H | 1 |
| Kawada, A | 1 |
| Mitsuhashi, Y | 1 |
| Hanada, K | 1 |
1 other study available for thymine and Protoporphyria, Erythropoietic
| Article | Year |
|---|---|
Novel ferrochelatase mutations in Japanese patients with erythropoietic protoporphyria: high frequency of the splice site modulator IVS3-48C polymorphism in the Japanese population.
Topics: Asian People; Cytosine; DNA, Recombinant; Ferrochelatase; Humans; Introns; Mutation; Pedigree; Polym | 2006 |