thymine has been researched along with Cochlear Hearing Loss in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Lehtonen, MS | 1 |
| Moilanen, JS | 1 |
| Majamaa, K | 1 |
| Leshinsky-Silver, E | 1 |
| Berman, Z | 1 |
| Vinkler, C | 1 |
| Yannov-Sharav, M | 1 |
| Lev, D | 1 |
| Kobayashi, K | 1 |
| Oguchi, T | 1 |
| Asamura, K | 1 |
| Miyagawa, M | 1 |
| Horai, S | 1 |
| Abe, S | 1 |
| Usami, S | 1 |
3 other studies available for thymine and Cochlear Hearing Loss
| Article | Year |
|---|---|
Increased variation in mtDNA in patients with familial sensorineural hearing impairment.
Topics: Adenine; Adult; Case-Control Studies; Cytosine; DNA, Mitochondrial; Europe; Female; Finland; Genetic | 2003 |
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness.
Topics: Alleles; Base Sequence; Child; Connexin 26; Connexins; Conserved Sequence; Cytosine; Female; Genes, | 2005 |
Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.
Topics: Adolescent; Adult; Aged; Aminoglycosides; Case-Control Studies; Child; Child, Preschool; DNA, Mitoch | 2005 |