adenine has been researched along with Gyrate Atrophy in 1 studies
Gyrate Atrophy: Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.
| 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 |
|---|---|
| Mashima, Y | 1 |
| Weleber, RG | 1 |
| Kennaway, NG | 1 |
| Inana, G | 1 |
1 other study available for adenine and Gyrate Atrophy
| Article | Year |
|---|---|
A single-base change at a splice acceptor site in the ornithine aminotransferase gene causes abnormal RNA splicing in gyrate atrophy.
Topics: Adenine; Base Sequence; DNA; Female; Guanine; Gyrate Atrophy; Humans; Molecular Sequence Data; Mutat | 1992 |