thymidine has been researched along with Complex IV Deficiency in 1 studies
Excerpt | Relevance | Reference |
---|---|---|
"We identified a single thymidine insertion at nucleotide position 5537 (T5537i) in the mitochondrial DNA transfer RNA gene for tryptophan in a family in which the proband had a progressive neurological disorder and his brother died in infancy of Leigh syndrome." | 3.69 | Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene. ( De Vivo, DC; DiMauro, S; El-Shahawi, M; Kranz-Eble, P; Sano, M; Santorelli, FM; Shanske, S; Tanji, K, 1997) |
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 |
---|---|
Santorelli, FM | 1 |
Tanji, K | 1 |
Sano, M | 1 |
Shanske, S | 1 |
El-Shahawi, M | 1 |
Kranz-Eble, P | 1 |
DiMauro, S | 1 |
De Vivo, DC | 1 |
1 other study available for thymidine and Complex IV Deficiency
Article | Year |
---|---|
Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene.
Topics: Adult; Animals; Autopsy; Base Sequence; Child; Cytochrome-c Oxidase Deficiency; DNA Transposable Ele | 1997 |