Early diagnosis and management of cardiac manifestations in mucopolysaccharidoses: a practical guide for paediatric and adult cardiologists
Abstract Mucopolysaccharidoses (MPS) are a group of hereditary disorders caused by lysosomal storage of glycosaminoglycans (GAGs) and characterized by a wide variability of phenotypes from severe fetal-neonatal forms to attenuated diseases diagnosed in adult individuals. The clinical picture general...
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| Main Authors: | , , |
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| Format: | Book |
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BMC,
2018-11-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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