glycine has been researched along with Color Vision Defects in 3 studies
Color Vision Defects: Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Rosenberg, T | 1 |
| Baumann, B | 1 |
| Kohl, S | 1 |
| Zrenner, E | 2 |
| Jorgensen, AL | 1 |
| Wissinger, B | 1 |
| Weitz, CJ | 1 |
| Miyake, Y | 1 |
| Shinzato, K | 1 |
| Montag, E | 1 |
| Went, LN | 1 |
| Nathans, J | 1 |
| Tancredi, F | 1 |
| Guazzi, G | 1 |
| Auricchio, S | 1 |
3 other studies available for glycine and Color Vision Defects
| Article | Year |
|---|---|
Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations.
Topics: Adolescent; Adult; Alanine; Animals; Base Sequence; Chlorocebus aethiops; Color Perception; Color Vi | 2004 |
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin.
Topics: Arginine; Base Sequence; Chi-Square Distribution; Cloning, Molecular; Color Vision Defects; DNA; DNA | 1992 |
Renal iminoglycinuria without intestinal malabsorption of glycine and imino acids.
Topics: Amblyopia; Child; Color Vision Defects; Female; Glycine; Heterozygote; Homozygote; Humans; Hydroxypr | 1970 |