histidine has been researched along with Leigh Disease in 1 studies
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 |
---|---|
Joshi, MB; Rajshekher, GP; Reddy, AG; Singh, L; Thangaraj, K; Vanniarajan, A | 1 |
1 other study(ies) available for histidine and Leigh Disease
Article | Year |
---|---|
Novel mitochondrial mutation in the ND4 gene associated with Leigh syndrome.
Topics: Amino Acid Sequence; Amino Acid Substitution; Basal Ganglia; Basal Ganglia Diseases; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex I; Female; Genetic Predisposition to Disease; Histidine; Humans; Infant; Leigh Disease; Magnetic Resonance Imaging; Molecular Sequence Data; Mutation, Missense; Protein Subunits; Tyrosine | 2006 |