tryptophan has been researched along with Choroid Diseases in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Deutman, AF; Heutink, P; Hoyng, CB; Oostra, BA; Pinckers, A; Testers, L | 1 |
1 other study(ies) available for tryptophan and Choroid Diseases
Article | Year |
---|---|
Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene.
Topics: Adult; Aged; Amino Acid Sequence; Arginine; Base Sequence; Choroid Diseases; Codon; DNA; DNA Mutational Analysis; DNA Primers; Eye Proteins; Female; Fluorescein Angiography; Fundus Oculi; Humans; Intermediate Filament Proteins; Male; Membrane Glycoproteins; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Pedigree; Peripherins; Point Mutation; Polymerase Chain Reaction; Retinal Degeneration; Tryptophan | 1996 |