glycine has been researched along with Eye Abnormalities in 2 studies
Eye Abnormalities: Congenital absence of or defects in structures of the eye; may also be hereditary.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Diffuse leukoencephalopathy associated with ocular malformations of the Axenfeld-Rieger type was observed in five individuals." | 1.34 | COL4A1 mutation in Axenfeld-Rieger anomaly with leukoencephalopathy and stroke. ( Arveiler, B; Bouchet, JP; Burgelin, I; Calvas, P; Coupry, I; Dousset, V; Goizet, C; Gorry, P; Lacombe, D; Menegon, P; Orgogozo, JM; Orignac, I; Sibon, I, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zhou, G | 1 |
| Zhou, N | 1 |
| Hu, S | 1 |
| Zhao, L | 1 |
| Zhang, C | 1 |
| Qi, Y | 1 |
| Sibon, I | 1 |
| Coupry, I | 1 |
| Menegon, P | 1 |
| Bouchet, JP | 1 |
| Gorry, P | 1 |
| Burgelin, I | 1 |
| Calvas, P | 1 |
| Orignac, I | 1 |
| Dousset, V | 1 |
| Lacombe, D | 1 |
| Orgogozo, JM | 1 |
| Arveiler, B | 1 |
| Goizet, C | 1 |
2 other studies available for glycine and Eye Abnormalities
| Article | Year |
|---|---|
A missense mutation in CRYBA4 associated with congenital cataract and microcornea.
Topics: Adolescent; Adult; Amino Acid Substitution; Base Sequence; beta-Crystallin A Chain; Cataract; Child; | 2010 |
COL4A1 mutation in Axenfeld-Rieger anomaly with leukoencephalopathy and stroke.
Topics: Adult; Anterior Eye Segment; Aspartic Acid; Autoantigens; Brain Diseases; Child; Collagen Type IV; E | 2007 |