methionine has been researched along with Corneal Dystrophies 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 |
|---|---|
| Al-Rajhi, A; Brandt, JD; Fingert, JH; Mannis, MJ; Roos, B; Shah, SS; Sheffield, VC; Stone, EM; Syed, NA | 1 |
| Afshari, NA; Bahadur, RP; Eifrig, DE; Enghild, JJ; Klintworth, GK; Thogersen, IB | 1 |
2 other study(ies) available for methionine and Corneal Dystrophies
| Article | Year |
|---|---|
Mutation in the SLC4A11 gene associated with autosomal recessive congenital hereditary endothelial dystrophy in a large Saudi family.
Topics: Anion Transport Proteins; Antiporters; Arabs; Cohort Studies; Corneal Dystrophies, Hereditary; Endothelium, Corneal; Female; Genes, Recessive; Homozygote; Humans; Male; Methionine; Mutation; Pedigree; Saudi Arabia; Threonine | 2008 |
Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene.
Topics: Base Sequence; Corneal Dystrophies, Hereditary; Extracellular Matrix Proteins; Homozygote; Humans; Male; Methionine; Middle Aged; Mutation; Transforming Growth Factor beta; Valine | 2008 |