tryptophan and Eye Diseases, Hereditary

tryptophan has been researched along with Eye Diseases, Hereditary in 1 studies

Research

Studies (1)

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

Authors	Studies
Bingham, EL; Hiriyanna, K; Kemp, J; Richards, J; Sieving, PA	1

Other Studies

1 other study(ies) available for tryptophan and Eye Diseases, Hereditary

Article	Year
Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave. American journal of ophthalmology, 1999, Volume: 128, Issue:2 Topics: Adolescent; Adult; Arginine; Diagnosis, Differential; DNA; Electroretinography; Exons; Eye Diseases, Hereditary; Eye Proteins; Genetic Linkage; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Polymerase Chain Reaction; Retina; Retinal Degeneration; Tryptophan; X Chromosome	1999

Article

Year

Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave.

American journal of ophthalmology, 1999, Volume: 128, Issue:2

Topics: Adolescent; Adult; Arginine; Diagnosis, Differential; DNA; Electroretinography; Exons; Eye Diseases, Hereditary; Eye Proteins; Genetic Linkage; Humans; Male; Middle Aged; Mutation, Missense; Pedigree; Polymerase Chain Reaction; Retina; Retinal Degeneration; Tryptophan; X Chromosome

1999