threonine has been researched along with Hereditary Optic Atrophy in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kalinin, VN; Olek, K; Poller, W; Schmidt, W | 1 |
| Batandier, C; Lunardi, J; Picard, A; Tessier, N | 1 |
2 other study(ies) available for threonine and Hereditary Optic Atrophy
| Article | Year |
|---|---|
[A new point mutation in the mitochondrial gene ND1, detected in a patient with type II diabetes].
Topics: Alanine; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Humans; NADH Dehydrogenase; Optic Atrophies, Hereditary; Point Mutation; Threonine | 1995 |
Identification of a novel T398A mutation in the ND5 subunit of the mitochondrial complex I and of three novel mtDNA polymorphisms in two patients presenting ocular symptoms.
Topics: Alanine; Amino Acid Substitution; DNA, Mitochondrial; Electron Transport Complex I; Female; Humans; Mutation; NADH, NADPH Oxidoreductases; Optic Atrophies, Hereditary; Polymorphism, Genetic; Polymorphism, Single Nucleotide; Threonine | 2000 |