glycine has been researched along with Mucopolysaccharidosis III in 1 studies
Mucopolysaccharidosis III: Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Jansen, AC | 1 |
| Cao, H | 1 |
| Kaplan, P | 1 |
| Silver, K | 1 |
| Leonard, G | 1 |
| De Meirleir, L | 1 |
| Lissens, W | 1 |
| Liebaers, I | 1 |
| Veilleux, M | 1 |
| Andermann, F | 1 |
| Hegele, RA | 1 |
| Andermann, E | 1 |
1 other study available for glycine and Mucopolysaccharidosis III
| Article | Year |
|---|---|
Sanfilippo syndrome type D: natural history and identification of 3 novel mutations in the GNS Gene.
Topics: Adolescent; Adult; Aspartic Acid; Disease Progression; DNA Mutational Analysis; Family Health; Femal | 2007 |