2-propanol has been researched along with Congenital Nystagmus in 4 studies
2-Propanol: An isomer of 1-PROPANOL. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.
propan-2-ol : A secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Aniridia is a rare panocular disorder characterized by iris hypoplasia and other associated eye anomalies." | 1.42 | Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia. ( Dubey, SK; Mahalaxmi, N; Sundaresan, P; Vijayalakshmi, P, 2015) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dubey, SK | 1 |
| Mahalaxmi, N | 1 |
| Vijayalakshmi, P | 1 |
| Sundaresan, P | 1 |
| Fang, S | 1 |
| Guo, X | 1 |
| Jia, X | 1 |
| Xiao, X | 1 |
| Li, S | 1 |
| Zhang, Q | 1 |
| Hu, J | 1 |
| Liang, D | 1 |
| Xue, J | 1 |
| Liu, J | 1 |
| Wu, L | 1 |
| Vincent, MC | 1 |
| Gallai, R | 1 |
| Olivier, D | 1 |
| Speeg-Schatz, C | 1 |
| Flament, J | 1 |
| Calvas, P | 1 |
| Dollfus, H | 1 |
4 other studies available for 2-propanol and Congenital Nystagmus
| Article | Year |
|---|---|
Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia.
Topics: Adolescent; Adult; Aged; Amino Acid Sequence; Aniridia; Base Sequence; Case-Control Studies; Catarac | 2015 |
Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism.
Topics: Adolescent; Adult; Albinism, Ocular; Asian People; Base Sequence; Child; Child, Preschool; China; DN | 2008 |
A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmus.
Topics: Adolescent; Adult; Asian People; Base Sequence; Child; China; DNA Mutational Analysis; Eye Proteins; | 2011 |
Variable phenotype related to a novel PAX 6 mutation (IVS4+5G>C) in a family presenting congenital nystagmus and foveal hypoplasia.
Topics: Adult; Amino Acid Sequence; Base Sequence; DNA Mutational Analysis; Eye Abnormalities; Eye Proteins; | 2004 |