Add to ORKGMucolipidosis type II (MLII, MIM 252500) is a lysosomal storage disorders caused by defects i
Background: At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lys...
A neonate presented with mucopolysaccharidosis-like phenotypic expression and typical signs of dyso...
Mucolipidosis type II (MLII) is a rare lysosomal storage disorder caused by defective trafficking o...
Mucolipidosis II (ML II) or inclusion cell disease (I-cell disease) is a rarely occurring autosomal ...
Mucolipidosis II (ML II or I-cell disease ) (OMIM 252500) is an autosomal recessive lysosomal enzyme...
UNLABELLED: Mucolipidosis II (ML II or I-cell disease ) (OMIM 252500) is an autosomal recessive lyso...
Background: Mucolipidosis types II and III (ML II/III) are autosomal recessive disorders caused by a...
Introduction. Lysosomal storage disorders (LSDs) are rare diseases with more than 50 different entit...
We analyzed placental tissue in one fetus with MPS II (iduronate sulphatase deficiency) and another ...
Introduction. Lysosomal storage disorders (LSDs) are rare diseases with more than 50 different entit...
Mucolipidosis type II (ML II) is an autosomal recessive lysosomal targeting disorder that may presen...
Purpose: Mucolipidosis (ML) II, MLIII alpha/beta, and MLIII gamma are rare autosomal recessive lysos...
Abstract Background Mucolipidosis II (ML II α/β) is an inherited lysosomal storage disorder caused b...
Placental mesenchymal dysplasia (PMD) is a rare placental disorder characterized by placental enlarg...
Contains fulltext : 50653.pdf (publisher's version ) (Closed access)BACKGROUND: At...
Background: At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lys...
A neonate presented with mucopolysaccharidosis-like phenotypic expression and typical signs of dyso...
Mucolipidosis type II (MLII) is a rare lysosomal storage disorder caused by defective trafficking o...
Mucolipidosis II (ML II) or inclusion cell disease (I-cell disease) is a rarely occurring autosomal ...
Mucolipidosis II (ML II or I-cell disease ) (OMIM 252500) is an autosomal recessive lysosomal enzyme...
UNLABELLED: Mucolipidosis II (ML II or I-cell disease ) (OMIM 252500) is an autosomal recessive lyso...
Background: Mucolipidosis types II and III (ML II/III) are autosomal recessive disorders caused by a...
Introduction. Lysosomal storage disorders (LSDs) are rare diseases with more than 50 different entit...
We analyzed placental tissue in one fetus with MPS II (iduronate sulphatase deficiency) and another ...
Introduction. Lysosomal storage disorders (LSDs) are rare diseases with more than 50 different entit...
Mucolipidosis type II (ML II) is an autosomal recessive lysosomal targeting disorder that may presen...
Purpose: Mucolipidosis (ML) II, MLIII alpha/beta, and MLIII gamma are rare autosomal recessive lysos...
Abstract Background Mucolipidosis II (ML II α/β) is an inherited lysosomal storage disorder caused b...
Placental mesenchymal dysplasia (PMD) is a rare placental disorder characterized by placental enlarg...
Contains fulltext : 50653.pdf (publisher's version ) (Closed access)BACKGROUND: At...
Background: At least 20 inborn errors of metabolism may cause hydrops fetalis. Most of these are lys...
A neonate presented with mucopolysaccharidosis-like phenotypic expression and typical signs of dyso...
Mucolipidosis type II (MLII) is a rare lysosomal storage disorder caused by defective trafficking o...