glycine has been researched along with Mucopolysaccharidosis VI in 1 studies
Mucopolysaccharidosis VI: Mucopolysaccharidosis with excessive CHONDROITIN SULFATE B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-ACETYLGALACTOSAMINE-4-SULFATASE (arylsulfatase B).
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (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 |
|---|---|
| Wicker, G | 1 |
| Prill, V | 1 |
| Brooks, D | 1 |
| Gibson, G | 1 |
| Hopwood, J | 1 |
| von Figura, K | 1 |
| Peters, C | 1 |
1 other study available for glycine and Mucopolysaccharidosis VI
| Article | Year |
|---|---|
Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). An intermediate clinical phenotype caused by substitution of valine for glycine at position 137 of arylsulfatase B.
Topics: Alleles; Amino Acid Sequence; Base Sequence; Blotting, Western; Cell Line; Chondro-4-Sulfatase; Clon | 1991 |