arginine has been researched along with Mucopolysaccharidosis VI in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Arlt, G; Brooks, DA; Hopwood, JJ; Isbrandt, D; Peters, C; von Figura, K | 1 |
| Chang, JG; Lee, CC; Tsai, FJ; Wu, JY; Yang, CF | 1 |
2 other study(ies) available for arginine and Mucopolysaccharidosis VI
| Article | Year |
|---|---|
Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): six unique arylsulfatase B gene alleles causing variable disease phenotypes.
Topics: Alleles; Amino Acid Sequence; Animals; Arginine; Base Sequence; Cell Line; Cells, Cultured; Child, Preschool; Chondro-4-Sulfatase; Chromosome Mapping; Consanguinity; Cysteine; DNA; DNA Primers; DNA Transposable Elements; Exons; Female; Humans; Infant; Leucine; Male; Molecular Sequence Data; Mucopolysaccharidosis VI; Phenotype; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Proline; Restriction Mapping; Sequence Deletion; Transfection | 1994 |
A novel mutation (Q239R) identified in a Taiwan Chinese patient with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome).
Topics: Alleles; Amino Acid Substitution; Arginine; Asian People; China; Genes, Recessive; Germ-Line Mutation; Glutamine; Humans; Mucopolysaccharidosis VI; Mutation, Missense; N-Acetylgalactosamine-4-Sulfatase; Syndrome; Taiwan | 2000 |