phenylalanine and Congenital Nystagmus

phenylalanine has been researched along with Congenital Nystagmus in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gu, F; He, X; Huang, S; Ma, X; Wang, Y; Yan, J; Zhang, M1

Other Studies

1 other study(ies) available for phenylalanine and Congenital Nystagmus

ArticleYear
A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family.
    Molecular vision, 2008, Jan-11, Volume: 14

    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