glutamic acid has been researched along with Fabry Disease in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (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 |
|---|---|
| Ishii, S; Kase, R; Sakuraba, H; Suzuki, Y | 1 |
| Kajita, M; Miyazaki, T; Mizutani, N; Murata, Y; Niwa, T; Ohmori, S; Seo, H | 1 |
2 other study(ies) available for glutamic acid and Fabry Disease
| Article | Year |
|---|---|
Characterization of a mutant alpha-galactosidase gene product for the late-onset cardiac form of Fabry disease.
Topics: Age of Onset; alpha-Galactosidase; Amino Acid Sequence; Animals; Cell Line; Enzyme Stability; Fabry Disease; Galactose; Gene Expression; Genetic Variation; Glutamates; Glutamic Acid; Glutamine; Humans; Hydrogen-Ion Concentration; Kinetics; Lymphocytes; Melibiose; Point Mutation; Recombinant Proteins; Thermodynamics; Transfection | 1993 |
A novel mutation (E358K) in the alpha-galactosidase A gene detected in a Japanese family with Fabry disease.
Topics: Adolescent; Adult; alpha-Galactosidase; Amino Acid Substitution; Base Sequence; DNA; DNA Mutational Analysis; Fabry Disease; Family Health; Female; Glutamic Acid; Humans; Japan; Lysine; Male; Mutation; Pedigree; Point Mutation | 1998 |