tryptophan has been researched along with Encephalomyopathies, Mitochondrial 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 | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Karlsson, A; Larsson, NG; Lesko, N; Naess, K; Nennesmo, I; Solaroli, N; von Döbeln, U; Wibom, R | 1 |
1 other study(ies) available for tryptophan and Encephalomyopathies, Mitochondrial
Article | Year |
---|---|
Two novel mutations in thymidine kinase-2 cause early onset fatal encephalomyopathy and severe mtDNA depletion.
Topics: Adenosine Triphosphate; Arginine; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial; Female; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Male; Mitochondria; Mitochondria, Muscle; Mitochondrial Diseases; Mitochondrial Encephalomyopathies; Muscle, Skeletal; Mutagenesis, Site-Directed; Mutation; Thymidine Kinase; Tryptophan | 2010 |