lysine has been researched along with Microphthalmia in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kutsche, K; Shaw, GM; Wimplinger, I | 1 |
| Chylíková, B; Kren, V; Liska, F; Martínek, J | 1 |
2 other study(ies) available for lysine and Microphthalmia
| Article | Year |
|---|---|
HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations?
Topics: Abnormalities, Multiple; Adenine; Amino Acid Substitution; Animals; CHO Cells; Chromosomes, Human, X; Cohort Studies; Cornea; Cricetinae; Cricetulus; Eye Abnormalities; Female; Glutamic Acid; Guanine; Heterozygote; Humans; Lyases; Lysine; Microphthalmos; Mutation, Missense; Point Mutation; Saccharomyces cerevisiae; Severity of Illness Index; Transfection; X Chromosome Inactivation | 2007 |
Microphthalmia and cataract in rats with a novel point mutation in connexin 50 - L7Q.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Cataract; Chromosome Mapping; Connexins; Eye Proteins; Glutamine; Inheritance Patterns; Lens, Crystalline; Lysine; Microphthalmos; Molecular Sequence Data; Phenotype; Point Mutation; Rats | 2008 |