valine and ARSB Deficiency

valine has been researched along with ARSB Deficiency in 1 studies

Research

Studies (1)

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

Authors	Studies
Brooks, D; Gibson, G; Hopwood, J; Peters, C; Prill, V; von Figura, K; Wicker, G	1

Other Studies

1 other study(ies) available for valine and ARSB Deficiency

Article	Year
Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). An intermediate clinical phenotype caused by substitution of valine for glycine at position 137 of arylsulfatase B. The Journal of biological chemistry, 1991, Nov-15, Volume: 266, Issue:32 Topics: Alleles; Amino Acid Sequence; Base Sequence; Blotting, Western; Cell Line; Chondro-4-Sulfatase; Cloning, Molecular; Glycine; Humans; Kinetics; Molecular Sequence Data; Mucopolysaccharidosis VI; Mutagenesis, Site-Directed; Mutation; Oligodeoxyribonucleotides; Phenotype; Polymerase Chain Reaction; Recombinant Proteins; Restriction Mapping; RNA; Valine	1991

Article

Year

Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). An intermediate clinical phenotype caused by substitution of valine for glycine at position 137 of arylsulfatase B.

The Journal of biological chemistry, 1991, Nov-15, Volume: 266, Issue:32

Topics: Alleles; Amino Acid Sequence; Base Sequence; Blotting, Western; Cell Line; Chondro-4-Sulfatase; Cloning, Molecular; Glycine; Humans; Kinetics; Molecular Sequence Data; Mucopolysaccharidosis VI; Mutagenesis, Site-Directed; Mutation; Oligodeoxyribonucleotides; Phenotype; Polymerase Chain Reaction; Recombinant Proteins; Restriction Mapping; RNA; Valine

1991