Hurler disease (mucopolysaccharidosis type IH): clinical features and consanguinity in Tunisian population
<p>Abstract</p> <p>Mucopolysaccharidosis type I (MPS I) was a group of rare autosomal recessive disorder caused by the deficiency of the lysosomal enzyme, alpha -L -iduronidase, and the resulting accumulation of undergraded dematan sulfate and heparan sulfate. MPS I patients have a...
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| Main Authors: | , , , , , , , |
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| Format: | Book |
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BMC,
2011-11-01T00:00:00Z.
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