A RARE CASE OF HUNTER SYNDROME - CASE REPORT

Mucopolysaccharidoses (MPSs) are a group of rare genetic disorders within the larger family of lysosomal diseases. MPSs disorders are caused by a defi ciency in the activity of a specifi c lysosomal enzyme required for the degradation of glycosaminoglycans (GAGs). MPS type II, also called Hunter syn...

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Bibliographic Details
Main Authors: Lorena Elena Melit (Author), Oana Marginean (Author), Carmen Duicu (Author), Cristina Campean (Author), Maria Oana Marginean (Author)
Format: Book
Published: Amaltea Medical Publishing House, 2015-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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