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Mucopolysaccharidosis type I (MPSI) is a rare autosomal recessive disorder caused by mutations in th...
Mucopolysaccharidosis (MPS) types IIIA, B, C, and D are a group of autosomal recessive lysosomal sto...
We describe the clinical and pathologic findings in a murine model of mucopolysaccharidosis VII (Sly...
Murine mucopolysaccharidosis type VII is a heritable disease caused by a spontaneous mutation, gus(m...
We have characterized a new mutant mouse that has virtually no beta-glucuronidase activity. This bio...
Bibliography: p. 252-281.xiii, 281, [110] p., [11] leaves of plates : ill. ; 35 cm.Identifies and an...
Bibliography: p. 184-215.xvii, 215, [122] p., [21] leaves of plates : ill. ; 30 cm.Aims to clone the...
We present evidence that a 480G “)-A transition in the coding region of the P-glucuronidase gene, wh...
Mucopolysaccharidosis type I (MPS-I) is an autosomal recessive disease caused by mutations in the al...
The study of rare genetic diseases presents unique opportunity to uncover the genetic and molecular ...
Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) is a lysosomal storage disorder caus...
Here, we present the molecular diagnosis of a patient with a general clinical suspicion of Mucopolys...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is an X-linked genetic disorder caused by a ...
Objective(s): Mucopolysaccharidosis VI (MPS VI) or Maroteaux-Lamy syndrome is a rare metabolic disor...
BACKGROUND: Mucopolysaccharidosis type VI (MPS VI; Maroteaux -Lamy syndrome) is an autosomal recessi...
Mucopolysaccharidosis type I (MPSI) is a rare autosomal recessive disorder caused by mutations in th...
Mucopolysaccharidosis (MPS) types IIIA, B, C, and D are a group of autosomal recessive lysosomal sto...
We describe the clinical and pathologic findings in a murine model of mucopolysaccharidosis VII (Sly...
Murine mucopolysaccharidosis type VII is a heritable disease caused by a spontaneous mutation, gus(m...
We have characterized a new mutant mouse that has virtually no beta-glucuronidase activity. This bio...
Bibliography: p. 252-281.xiii, 281, [110] p., [11] leaves of plates : ill. ; 35 cm.Identifies and an...
Bibliography: p. 184-215.xvii, 215, [122] p., [21] leaves of plates : ill. ; 30 cm.Aims to clone the...
We present evidence that a 480G “)-A transition in the coding region of the P-glucuronidase gene, wh...
Mucopolysaccharidosis type I (MPS-I) is an autosomal recessive disease caused by mutations in the al...
The study of rare genetic diseases presents unique opportunity to uncover the genetic and molecular ...
Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) is a lysosomal storage disorder caus...
Here, we present the molecular diagnosis of a patient with a general clinical suspicion of Mucopolys...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is an X-linked genetic disorder caused by a ...
Objective(s): Mucopolysaccharidosis VI (MPS VI) or Maroteaux-Lamy syndrome is a rare metabolic disor...
BACKGROUND: Mucopolysaccharidosis type VI (MPS VI; Maroteaux -Lamy syndrome) is an autosomal recessi...
Mucopolysaccharidosis type I (MPSI) is a rare autosomal recessive disorder caused by mutations in th...
Mucopolysaccharidosis (MPS) types IIIA, B, C, and D are a group of autosomal recessive lysosomal sto...
We describe the clinical and pathologic findings in a murine model of mucopolysaccharidosis VII (Sly...