glycine has been researched along with AGA Deficiency in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 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 |
|---|---|
| Coulter-Mackie, MB | 1 |
| Brady, RO | 1 |
2 other studies available for glycine and AGA Deficiency
| Article | Year |
|---|---|
A novel exonic mutation in the aspartylglucosaminidase gene causes exon skipping.
Topics: Aspartic Acid; Aspartylglucosaminuria; Aspartylglucosylaminase; Exons; Glycine; Humans; Mutation, Mi | 1999 |
Inherited metabolic diseases of the nervous system.
Topics: Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors | 1976 |