arginine has been researched along with Amelogenesis Imperfecta 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 |
---|---|
Ariga, T; Kida, M; Matsuda, A; Minamitake, S; Ochi, H; Sakiyama, Y; Sekiguchi, H; Takabayashi, S | 1 |
BriceƱo, I; Chaves, M; Gutierrez, SJ; Torres, DM | 1 |
2 other study(ies) available for arginine and Amelogenesis Imperfecta
Article | Year |
---|---|
A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta.
Topics: Amelogenesis Imperfecta; Amelogenin; Arginine; Cytosine; Dental Enamel; Exons; Female; Genetic Diseases, X-Linked; Guanine; Heterozygote; Humans; Male; Mutation, Missense; Pedigree; Proline; Spectrometry, X-Ray Emission; X-Ray Diffraction | 2007 |
Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta.
Topics: Alleles; Amelogenesis Imperfecta; Arginine; Codon; Dental Enamel Proteins; Exons; Female; Genes, Dominant; Genotype; Guanine; Humans; Male; Methionine; Mutation; Pedigree; Phenotype; Thymine | 2007 |