arginine has been researched along with Autosomal Dominant Optic Atrophy 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 |
|---|---|
| Ge, J; Katz, BJ; Kosmorsky, G; Li, C; Traboulsi, EI; Zhang, K | 1 |
| Caporossi, A; Cardaioli, E; Da Pozzo, P; Dotti, MT; Federico, A; Franceschini, R; Gallus, GN; Motolese, E; Rufa, A | 1 |
2 other study(ies) available for arginine and Autosomal Dominant Optic Atrophy
| Article | Year |
|---|---|
Optic atrophy and sensorineural hearing loss in a family caused by an R445H OPA1 mutation.
Topics: Adult; Amino Acid Substitution; Arginine; Child; Female; Genetic Linkage; GTP Phosphohydrolases; Haplotypes; Hearing Loss, Sensorineural; Hearing Tests; Histidine; Humans; Male; Middle Aged; Mutation; Optic Atrophy, Autosomal Dominant | 2005 |
A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy.
Topics: Adult; Arginine; Codon, Nonsense; DNA Mutational Analysis; Exons; Family Health; Female; GTP Phosphohydrolases; Humans; Male; Mutation; Optic Atrophy, Autosomal Dominant | 2006 |