Mucopolysaccharidoses: early diagnostic signs in infants and children
Abstract Mucopolysaccharidoses (MPS) comprise a group of lysosomal disorders that are characterized by progressive, systemic clinical manifestations and a coarse phenotype. The different types, having clinical, biochemical, and genetic heterogeneity, share key clinical features in varying combinatio...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
BMC,
2018-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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