lysine has been researched along with Hereditary Optic Atrophy in 1 studies
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 |
---|---|
Barquera, B; Finel, M; Wikström, M; Zickermann, V | 1 |
1 other study(ies) available for lysine and Hereditary Optic Atrophy
Article | Year |
---|---|
Analysis of the pathogenic human mitochondrial mutation ND1/3460, and mutations of strictly conserved residues in its vicinity, using the bacterium Paracoccus denitrificans.
Topics: Alanine; Amino Acid Sequence; Animals; Aspartic Acid; Conserved Sequence; DNA, Mitochondrial; Electron Transport Complex I; Glutamine; Humans; Lysine; Molecular Sequence Data; Mutagenesis, Site-Directed; NAD(P)H Dehydrogenase (Quinone); NADH, NADPH Oxidoreductases; Optic Atrophies, Hereditary; Paracoccus denitrificans; Quinone Reductases | 1998 |