Molecular analysis of iduronate -2- sulfatase gene in Tunisian patients with mucopolysaccharidosis type II
<p>Abstract</p> <p>Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is X-linked recessive lysosomal storage disorder resulting from the defective activity of the enzyme iduronate-2-sulfatase (IDS). Hunter disease can vary from mild to severe, depending on the level of enzyme...
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| Main Authors: | , , , , , , , , |
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| Format: | Book |
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BMC,
2011-05-01T00:00:00Z.
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