phenylalanine has been researched along with Congenital Nystagmus in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Gu, F; He, X; Huang, S; Ma, X; Wang, Y; Yan, J; Zhang, M | 1 |
1 other study(ies) available for phenylalanine and Congenital Nystagmus
Article | Year |
---|---|
A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family.
Topics: Adult; Alleles; Amino Acid Substitution; Asian People; Base Sequence; Child; Chromosomes, Human, X; Cysteine; Cytoskeletal Proteins; DNA Mutational Analysis; Female; Genetic Diseases, X-Linked; Guanine; Humans; Male; Membrane Proteins; Mutation; Nystagmus, Congenital; Pedigree; Phenylalanine; Thymine | 2008 |