arginine and ARSB Deficiency

arginine has been researched along with ARSB Deficiency in 2 studies

Research

Studies (2)

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

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

Other Studies

2 other study(ies) available for arginine and ARSB Deficiency

Article	Year
Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): six unique arylsulfatase B gene alleles causing variable disease phenotypes. American journal of human genetics, 1994, Volume: 54, Issue:3 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). Human mutation, 2000, Volume: 15, Issue:4 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

Article

Year

Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): six unique arylsulfatase B gene alleles causing variable disease phenotypes.

American journal of human genetics, 1994, Volume: 54, Issue:3

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).

Human mutation, 2000, Volume: 15, Issue:4

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