glutamic acid has been researched along with Cockayne-Touraine Disease 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 |
|---|---|
| Ishiko, A; Masunaga, T; Murata, T; Nishikawa, T; Shimizu, H | 1 |
| Ee, HL; Goh, CL; Liu, L; McGrath, JA | 1 |
1 review(s) available for glutamic acid and Cockayne-Touraine Disease
| Article | Year |
|---|---|
Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa.
Topics: Adolescent; Adult; Amino Acid Substitution; Asian People; Child; Collagen Type VII; Diagnosis, Differential; Epidermolysis Bullosa Dystrophica; Female; Genes, Dominant; Genetic Predisposition to Disease; Glutamic Acid; Glycine; Heterozygote; Humans; Male; Middle Aged; Mutation; Pedigree | 2007 |
1 other study(ies) available for glutamic acid and Cockayne-Touraine Disease
| Article | Year |
|---|---|
Differences in recurrent COL7A1 mutations in dystrophic epidermolysis bullosa: ethnic-specific and worldwide recurrent mutations.
Topics: Alanine; Arginine; Asian People; Collagen Type VII; Cysteine; Epidermolysis Bullosa Dystrophica; Gene Deletion; Gene Frequency; Global Health; Glutamic Acid; Glycine; Humans; Japan; Mutation; Recurrence; United Kingdom | 2004 |